Canonical Allele Identifier: CA2245700497
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221700_7221701delinsGA , CM000679.2:g.7221700_7221701delinsGA GRCh38
NC_000017.10:g.7125019_7125020delinsGA , CM000679.1:g.7125019_7125020delinsGA GRCh37
NC_000017.9:g.7065743_7065744delinsGA NCBI36
NG_007975.1:g.6867_6868delinsGA
NG_008391.2:g.3350_3351delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.622+18_622+19delinsGA MANE Select ENSP00000349297.5:n.622+18_622+19delinsGA
ENST00000322910.9:c.*577+18_*577+19delinsGA ENSP00000325395.5:n.*577+18_*577+19delinsGA
ENST00000350303.9:c.556+18_556+19delinsGA ENSP00000344152.5:n.556+18_556+19delinsGA
ENST00000356839.9:c.622+18_622+19delinsGA ENSP00000349297.5:n.622+18_622+19delinsGA
ENST00000543245.6:c.691+18_691+19delinsGA ENSP00000438689.2:n.691+18_691+19delinsGA
ENST00000577191.5:n.699+18_699+19delinsGA
ENST00000577857.5:n.438+18_438+19delinsGA
ENST00000579286.5:n.803+18_803+19delinsGA
ENST00000579886.2:c.460+18_460+19delinsGA ENSP00000463246.1:n.460+18_460+19delinsGA
ENST00000580365.1:n.353+18_353+19delinsGA
ENST00000581378.5:c.340+18_340+19delinsGA
ENST00000581562.5:n.525-252_525-251delinsGA
ENST00000583312.5:c.622+18_622+19delinsGA ENSP00000467920.1:n.622+18_622+19delinsGA
ENST00000583760.1:n.404+18_404+19delinsGA
NM_000018.3:c.622+18_622+19delinsGA NP_000009.1:n.622+18_622+19delinsGA
NM_001033859.2:c.556+18_556+19delinsGA NP_001029031.1:n.556+18_556+19delinsGA
NM_001270447.1:c.691+18_691+19delinsGA NP_001257376.1:n.691+18_691+19delinsGA
NM_001270448.1:c.394+18_394+19delinsGA NP_001257377.1:n.394+18_394+19delinsGA
XM_006721516.2:c.622+18_622+19delinsGA XP_006721579.2:n.622+18_622+19delinsGA
XM_011523829.1:c.622+18_622+19delinsGA XP_011522131.1:n.622+18_622+19delinsGA
XM_011523830.1:c.622+18_622+19delinsGA XP_011522132.1:n.622+18_622+19delinsGA
XR_934021.1:n.729+18_729+19delinsGA
XR_934022.1:n.729+18_729+19delinsGA
XR_934023.1:n.729+18_729+19delinsGA
XM_006721516.3:c.622+18_622+19delinsGA XP_006721579.2:n.622+18_622+19delinsGA
XM_011523829.2:c.622+18_622+19delinsGA XP_011522131.1:n.622+18_622+19delinsGA
XM_011523830.2:c.622+18_622+19delinsGA XP_011522132.1:n.622+18_622+19delinsGA
XM_024450741.1:c.622+18_622+19delinsGA XP_024306509.1:n.622+18_622+19delinsGA
XR_934021.2:n.681+18_681+19delinsGA
XR_934022.2:n.681+18_681+19delinsGA
XR_934023.2:n.681+18_681+19delinsGA
NM_000018.4:c.622+18_622+19delinsGA MANE Select NP_000009.1:n.622+18_622+19delinsGA
NM_001033859.3:c.556+18_556+19delinsGA NP_001029031.1:n.556+18_556+19delinsGA
NM_001270447.2:c.691+18_691+19delinsGA NP_001257376.1:n.691+18_691+19delinsGA
NM_001270448.2:c.394+18_394+19delinsGA NP_001257377.1:n.394+18_394+19delinsGA