Canonical Allele Identifier: CA2245711802
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223748C= , CM000679.2:g.7223748C= GRCh38
NC_000017.10:g.7127067C= , CM000679.1:g.7127067C= GRCh37
NC_000017.9:g.7067791C= NCBI36
NG_007975.1:g.8915C=
NG_008391.2:g.1303G=
NG_033038.1:g.15797G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1269+18C= MANE Select ENSP00000349297.5:n.1269+18C=
ENST00000322910.9:c.*1224+18C= ENSP00000325395.5:n.*1224+18C=
ENST00000350303.9:c.1203+18C= ENSP00000344152.5:n.1203+18C=
ENST00000356839.9:c.1269+18C= ENSP00000349297.5:n.1269+18C=
ENST00000542255.6:c.127+18C=
ENST00000543245.6:c.1338+18C= ENSP00000438689.2:n.1338+18C=
ENST00000578579.2:n.440+18C=
ENST00000578711.1:n.244C=
ENST00000578824.5:n.685+18C=
ENST00000579425.5:n.293+18C=
ENST00000579546.1:c.106+18C=
ENST00000583850.5:n.44+18C=
ENST00000583858.5:c.298+18C=
ENST00000585203.6:n.477+18C=
NM_000018.3:c.1269+18C= NP_000009.1:n.1269+18C=
NM_001033859.2:c.1203+18C= NP_001029031.1:n.1203+18C=
NM_001270447.1:c.1338+18C= NP_001257376.1:n.1338+18C=
NM_001270448.1:c.1041+18C= NP_001257377.1:n.1041+18C=
XM_006721516.2:c.1269+18C= XP_006721579.2:n.1269+18C=
XM_011523829.1:c.1269+18C= XP_011522131.1:n.1269+18C=
XM_011523830.1:c.1269+18C= XP_011522132.1:n.1269+18C=
XR_934021.1:n.1376+18C=
XR_934022.1:n.1376+18C=
XR_934023.1:n.1376+18C=
XM_006721516.3:c.1269+18C= XP_006721579.2:n.1269+18C=
XM_011523829.2:c.1269+18C= XP_011522131.1:n.1269+18C=
XM_011523830.2:c.1269+18C= XP_011522132.1:n.1269+18C=
XM_024450741.1:c.1269+18C= XP_024306509.1:n.1269+18C=
XR_934021.2:n.1328+18C=
XR_934022.2:n.1328+18C=
XR_934023.2:n.1328+18C=
NM_000018.4:c.1269+18C= MANE Select NP_000009.1:n.1269+18C=
NM_001033859.3:c.1203+18C= NP_001029031.1:n.1203+18C=
NM_001270447.2:c.1338+18C= NP_001257376.1:n.1338+18C=
NM_001270448.2:c.1041+18C= NP_001257377.1:n.1041+18C=