Canonical Allele Identifier: CA2635781413
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221758_7221759insAA , CM000679.2:g.7221758_7221759insAA GRCh38
NC_000017.10:g.7125077_7125078insAA , CM000679.1:g.7125077_7125078insAA GRCh37
NC_000017.9:g.7065801_7065802insAA NCBI36
NG_007975.1:g.6925_6926insAA
NG_008391.2:g.3293_3294insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.622+76_622+77insAA MANE Select ENSP00000349297.5:n.622+76_622+77insAA
ENST00000322910.9:c.*577+76_*577+77insAA ENSP00000325395.5:n.*577+76_*577+77insAA
ENST00000350303.9:c.556+76_556+77insAA ENSP00000344152.5:n.556+76_556+77insAA
ENST00000356839.9:c.622+76_622+77insAA ENSP00000349297.5:n.622+76_622+77insAA
ENST00000543245.6:c.691+76_691+77insAA ENSP00000438689.2:n.691+76_691+77insAA
ENST00000577191.5:n.699+76_699+77insAA
ENST00000577857.5:n.438+76_438+77insAA
ENST00000579286.5:n.803+76_803+77insAA
ENST00000579886.2:c.460+76_460+77insAA ENSP00000463246.1:n.460+76_460+77insAA
ENST00000580365.1:n.353+76_353+77insAA
ENST00000581378.5:c.340+76_340+77insAA
ENST00000581562.5:n.525-194_525-193insAA
ENST00000583312.5:c.622+76_622+77insAA ENSP00000467920.1:n.622+76_622+77insAA
ENST00000583760.1:n.404+76_404+77insAA
NM_000018.3:c.622+76_622+77insAA NP_000009.1:n.622+76_622+77insAA
NM_001033859.2:c.556+76_556+77insAA NP_001029031.1:n.556+76_556+77insAA
NM_001270447.1:c.691+76_691+77insAA NP_001257376.1:n.691+76_691+77insAA
NM_001270448.1:c.394+76_394+77insAA NP_001257377.1:n.394+76_394+77insAA
XM_006721516.2:c.622+76_622+77insAA XP_006721579.2:n.622+76_622+77insAA
XM_011523829.1:c.622+76_622+77insAA XP_011522131.1:n.622+76_622+77insAA
XM_011523830.1:c.622+76_622+77insAA XP_011522132.1:n.622+76_622+77insAA
XR_934021.1:n.729+76_729+77insAA
XR_934022.1:n.729+76_729+77insAA
XR_934023.1:n.729+76_729+77insAA
XM_006721516.3:c.622+76_622+77insAA XP_006721579.2:n.622+76_622+77insAA
XM_011523829.2:c.622+76_622+77insAA XP_011522131.1:n.622+76_622+77insAA
XM_011523830.2:c.622+76_622+77insAA XP_011522132.1:n.622+76_622+77insAA
XM_024450741.1:c.622+76_622+77insAA XP_024306509.1:n.622+76_622+77insAA
XR_934021.2:n.681+76_681+77insAA
XR_934022.2:n.681+76_681+77insAA
XR_934023.2:n.681+76_681+77insAA
NM_000018.4:c.622+76_622+77insAA MANE Select NP_000009.1:n.622+76_622+77insAA
NM_001033859.3:c.556+76_556+77insAA NP_001029031.1:n.556+76_556+77insAA
NM_001270447.2:c.691+76_691+77insAA NP_001257376.1:n.691+76_691+77insAA
NM_001270448.2:c.394+76_394+77insAA NP_001257377.1:n.394+76_394+77insAA