Canonical Allele Identifier: CA2635782216
Gene: ACADVL HGNC NCBI

Linked Data

gnomAD v4: 17-7223615-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223615C>A , CM000679.2:g.7223615C>A GRCh38
NC_000017.10:g.7126934C>A , CM000679.1:g.7126934C>A GRCh37
NC_000017.9:g.7067658C>A NCBI36
NG_007975.1:g.8782C>A
NG_008391.2:g.1436G>T
NG_033038.1:g.15930G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1183-29C>A MANE Select ENSP00000349297.5:n.1183-29C>A
ENST00000322910.9:c.*1138-29C>A ENSP00000325395.5:n.*1138-29C>A
ENST00000350303.9:c.1117-29C>A ENSP00000344152.5:n.1117-29C>A
ENST00000356839.9:c.1183-29C>A ENSP00000349297.5:n.1183-29C>A
ENST00000542255.6:c.41-29C>A
ENST00000543245.6:c.1252-29C>A ENSP00000438689.2:n.1252-29C>A
ENST00000578579.2:n.325C>A
ENST00000578711.1:n.111C>A
ENST00000578824.5:n.599-29C>A
ENST00000579425.5:n.207-29C>A
ENST00000579546.1:c.20-29C>A
ENST00000583858.5:c.212-29C>A
ENST00000585203.6:n.391-29C>A
NM_000018.3:c.1183-29C>A NP_000009.1:n.1183-29C>A
NM_001033859.2:c.1117-29C>A NP_001029031.1:n.1117-29C>A
NM_001270447.1:c.1252-29C>A NP_001257376.1:n.1252-29C>A
NM_001270448.1:c.955-29C>A NP_001257377.1:n.955-29C>A
XM_006721516.2:c.1183-29C>A XP_006721579.2:n.1183-29C>A
XM_011523829.1:c.1183-29C>A XP_011522131.1:n.1183-29C>A
XM_011523830.1:c.1183-29C>A XP_011522132.1:n.1183-29C>A
XR_934021.1:n.1290-29C>A
XR_934022.1:n.1290-29C>A
XR_934023.1:n.1290-29C>A
XM_006721516.3:c.1183-29C>A XP_006721579.2:n.1183-29C>A
XM_011523829.2:c.1183-29C>A XP_011522131.1:n.1183-29C>A
XM_011523830.2:c.1183-29C>A XP_011522132.1:n.1183-29C>A
XM_024450741.1:c.1183-29C>A XP_024306509.1:n.1183-29C>A
XR_934021.2:n.1242-29C>A
XR_934022.2:n.1242-29C>A
XR_934023.2:n.1242-29C>A
NM_000018.4:c.1183-29C>A MANE Select NP_000009.1:n.1183-29C>A
NM_001033859.3:c.1117-29C>A NP_001029031.1:n.1117-29C>A
NM_001270447.2:c.1252-29C>A NP_001257376.1:n.1252-29C>A
NM_001270448.2:c.955-29C>A NP_001257377.1:n.955-29C>A