Canonical Allele Identifier: CA2635780820
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221299_7221300insG , CM000679.2:g.7221299_7221300insG GRCh38
NC_000017.10:g.7124618_7124619insG , CM000679.1:g.7124618_7124619insG GRCh37
NC_000017.9:g.7065342_7065343insG NCBI36
NG_007975.1:g.6466_6467insG
NG_008391.2:g.3751_3752insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-239_478-238insG MANE Select ENSP00000349297.5:n.478-239_478-238insG
ENST00000322910.9:c.*433-239_*433-238insG ENSP00000325395.5:n.*433-239_*433-238insG
ENST00000350303.9:c.412-239_412-238insG ENSP00000344152.5:n.412-239_412-238insG
ENST00000356839.9:c.478-239_478-238insG ENSP00000349297.5:n.478-239_478-238insG
ENST00000543245.6:c.547-239_547-238insG ENSP00000438689.2:n.547-239_547-238insG
ENST00000577191.5:n.555-239_555-238insG
ENST00000577433.5:n.686-239_686-238insG
ENST00000577857.5:n.294-239_294-238insG
ENST00000579286.5:n.659-239_659-238insG
ENST00000579886.2:c.316-239_316-238insG ENSP00000463246.1:n.316-239_316-238insG
ENST00000580365.1:n.209-239_209-238insG
ENST00000581378.5:c.177-220_177-219insG
ENST00000581562.5:n.524+241_524+242insG
ENST00000582166.1:n.459-239_459-238insG
ENST00000583312.5:c.478-239_478-238insG ENSP00000467920.1:n.478-239_478-238insG
ENST00000583760.1:n.21_22insG
NM_000018.3:c.478-239_478-238insG NP_000009.1:n.478-239_478-238insG
NM_001033859.2:c.412-239_412-238insG NP_001029031.1:n.412-239_412-238insG
NM_001270447.1:c.547-239_547-238insG NP_001257376.1:n.547-239_547-238insG
NM_001270448.1:c.250-239_250-238insG NP_001257377.1:n.250-239_250-238insG
XM_006721516.2:c.478-239_478-238insG XP_006721579.2:n.478-239_478-238insG
XM_011523829.1:c.478-239_478-238insG XP_011522131.1:n.478-239_478-238insG
XM_011523830.1:c.478-239_478-238insG XP_011522132.1:n.478-239_478-238insG
XR_934021.1:n.585-239_585-238insG
XR_934022.1:n.585-239_585-238insG
XR_934023.1:n.585-239_585-238insG
XM_006721516.3:c.478-239_478-238insG XP_006721579.2:n.478-239_478-238insG
XM_011523829.2:c.478-239_478-238insG XP_011522131.1:n.478-239_478-238insG
XM_011523830.2:c.478-239_478-238insG XP_011522132.1:n.478-239_478-238insG
XM_024450741.1:c.478-239_478-238insG XP_024306509.1:n.478-239_478-238insG
XR_934021.2:n.537-239_537-238insG
XR_934022.2:n.537-239_537-238insG
XR_934023.2:n.537-239_537-238insG
NM_000018.4:c.478-239_478-238insG MANE Select NP_000009.1:n.478-239_478-238insG
NM_001033859.3:c.412-239_412-238insG NP_001029031.1:n.412-239_412-238insG
NM_001270447.2:c.547-239_547-238insG NP_001257376.1:n.547-239_547-238insG
NM_001270448.2:c.250-239_250-238insG NP_001257377.1:n.250-239_250-238insG