Canonical Allele Identifier: CA2245699676
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221342_7221346delinsAAGAC , CM000679.2:g.7221342_7221346delinsAAGAC GRCh38
NC_000017.10:g.7124661_7124665delinsAAGAC , CM000679.1:g.7124661_7124665delinsAAGAC GRCh37
NC_000017.9:g.7065385_7065389delinsAAGAC NCBI36
NG_007975.1:g.6509_6513delinsAAGAC
NG_008391.2:g.3705_3709delinsGTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-196_478-192delinsAAGAC MANE Select ENSP00000349297.5:n.478-196_478-192delinsAAGAC
ENST00000322910.9:c.*433-196_*433-192delinsAAGAC ENSP00000325395.5:n.*433-196_*433-192delinsAAGAC
ENST00000350303.9:c.412-196_412-192delinsAAGAC ENSP00000344152.5:n.412-196_412-192delinsAAGAC
ENST00000356839.9:c.478-196_478-192delinsAAGAC ENSP00000349297.5:n.478-196_478-192delinsAAGAC
ENST00000543245.6:c.547-196_547-192delinsAAGAC ENSP00000438689.2:n.547-196_547-192delinsAAGAC
ENST00000577191.5:n.555-196_555-192delinsAAGAC
ENST00000577433.5:n.686-196_686-192delinsAAGAC
ENST00000577857.5:n.294-196_294-192delinsAAGAC
ENST00000579286.5:n.659-196_659-192delinsAAGAC
ENST00000579886.2:c.316-196_316-192delinsAAGAC ENSP00000463246.1:n.316-196_316-192delinsAAGAC
ENST00000580365.1:n.209-196_209-192delinsAAGAC
ENST00000581378.5:c.177-177_177-173delinsAAGAC
ENST00000581562.5:n.524+284_524+288delinsAAGAC
ENST00000582166.1:n.459-196_459-192delinsAAGAC
ENST00000583312.5:c.478-196_478-192delinsAAGAC ENSP00000467920.1:n.478-196_478-192delinsAAGAC
ENST00000583760.1:n.64_68delinsAAGAC
NM_000018.3:c.478-196_478-192delinsAAGAC NP_000009.1:n.478-196_478-192delinsAAGAC
NM_001033859.2:c.412-196_412-192delinsAAGAC NP_001029031.1:n.412-196_412-192delinsAAGAC
NM_001270447.1:c.547-196_547-192delinsAAGAC NP_001257376.1:n.547-196_547-192delinsAAGAC
NM_001270448.1:c.250-196_250-192delinsAAGAC NP_001257377.1:n.250-196_250-192delinsAAGAC
XM_006721516.2:c.478-196_478-192delinsAAGAC XP_006721579.2:n.478-196_478-192delinsAAGAC
XM_011523829.1:c.478-196_478-192delinsAAGAC XP_011522131.1:n.478-196_478-192delinsAAGAC
XM_011523830.1:c.478-196_478-192delinsAAGAC XP_011522132.1:n.478-196_478-192delinsAAGAC
XR_934021.1:n.585-196_585-192delinsAAGAC
XR_934022.1:n.585-196_585-192delinsAAGAC
XR_934023.1:n.585-196_585-192delinsAAGAC
XM_006721516.3:c.478-196_478-192delinsAAGAC XP_006721579.2:n.478-196_478-192delinsAAGAC
XM_011523829.2:c.478-196_478-192delinsAAGAC XP_011522131.1:n.478-196_478-192delinsAAGAC
XM_011523830.2:c.478-196_478-192delinsAAGAC XP_011522132.1:n.478-196_478-192delinsAAGAC
XM_024450741.1:c.478-196_478-192delinsAAGAC XP_024306509.1:n.478-196_478-192delinsAAGAC
XR_934021.2:n.537-196_537-192delinsAAGAC
XR_934022.2:n.537-196_537-192delinsAAGAC
XR_934023.2:n.537-196_537-192delinsAAGAC
NM_000018.4:c.478-196_478-192delinsAAGAC MANE Select NP_000009.1:n.478-196_478-192delinsAAGAC
NM_001033859.3:c.412-196_412-192delinsAAGAC NP_001029031.1:n.412-196_412-192delinsAAGAC
NM_001270447.2:c.547-196_547-192delinsAAGAC NP_001257376.1:n.547-196_547-192delinsAAGAC
NM_001270448.2:c.250-196_250-192delinsAAGAC NP_001257377.1:n.250-196_250-192delinsAAGAC