Canonical Allele Identifier: CA2635781066
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221430_7221432del , CM000679.2:g.7221430_7221432del GRCh38
NC_000017.10:g.7124749_7124751del , CM000679.1:g.7124749_7124751del GRCh37
NC_000017.9:g.7065473_7065475del NCBI36
NG_007975.1:g.6597_6599del
NG_008391.2:g.3619_3621del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-108_478-106del MANE Select ENSP00000349297.5:n.478-108_478-106del
ENST00000322910.9:c.*433-108_*433-106del ENSP00000325395.5:n.*433-108_*433-106del
ENST00000350303.9:c.412-108_412-106del ENSP00000344152.5:n.412-108_412-106del
ENST00000356839.9:c.478-108_478-106del ENSP00000349297.5:n.478-108_478-106del
ENST00000543245.6:c.547-108_547-106del ENSP00000438689.2:n.547-108_547-106del
ENST00000577191.5:n.555-108_555-106del
ENST00000577433.5:n.686-108_686-106del
ENST00000577857.5:n.294-108_294-106del
ENST00000579286.5:n.659-108_659-106del
ENST00000579886.2:c.316-108_316-106del ENSP00000463246.1:n.316-108_316-106del
ENST00000580365.1:n.209-108_209-106del
ENST00000581378.5:c.177-89_177-87del
ENST00000581562.5:n.524+372_524+374del
ENST00000582166.1:n.459-108_459-106del
ENST00000583312.5:c.478-108_478-106del ENSP00000467920.1:n.478-108_478-106del
ENST00000583760.1:n.152_154del
NM_000018.3:c.478-108_478-106del NP_000009.1:n.478-108_478-106del
NM_001033859.2:c.412-108_412-106del NP_001029031.1:n.412-108_412-106del
NM_001270447.1:c.547-108_547-106del NP_001257376.1:n.547-108_547-106del
NM_001270448.1:c.250-108_250-106del NP_001257377.1:n.250-108_250-106del
XM_006721516.2:c.478-108_478-106del XP_006721579.2:n.478-108_478-106del
XM_011523829.1:c.478-108_478-106del XP_011522131.1:n.478-108_478-106del
XM_011523830.1:c.478-108_478-106del XP_011522132.1:n.478-108_478-106del
XR_934021.1:n.585-108_585-106del
XR_934022.1:n.585-108_585-106del
XR_934023.1:n.585-108_585-106del
XM_006721516.3:c.478-108_478-106del XP_006721579.2:n.478-108_478-106del
XM_011523829.2:c.478-108_478-106del XP_011522131.1:n.478-108_478-106del
XM_011523830.2:c.478-108_478-106del XP_011522132.1:n.478-108_478-106del
XM_024450741.1:c.478-108_478-106del XP_024306509.1:n.478-108_478-106del
XR_934021.2:n.537-108_537-106del
XR_934022.2:n.537-108_537-106del
XR_934023.2:n.537-108_537-106del
NM_000018.4:c.478-108_478-106del MANE Select NP_000009.1:n.478-108_478-106del
NM_001033859.3:c.412-108_412-106del NP_001029031.1:n.412-108_412-106del
NM_001270447.2:c.547-108_547-106del NP_001257376.1:n.547-108_547-106del
NM_001270448.2:c.250-108_250-106del NP_001257377.1:n.250-108_250-106del