Canonical Allele Identifier: CA2635782028
Gene: ACADVL HGNC NCBI

Linked Data

gnomAD v4: 17-7223480-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223480A>T , CM000679.2:g.7223480A>T GRCh38
NC_000017.10:g.7126799A>T , CM000679.1:g.7126799A>T GRCh37
NC_000017.9:g.7067523A>T NCBI36
NG_007975.1:g.8647A>T
NG_008391.2:g.1571T>A
NG_033038.1:g.16065T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1183-164A>T MANE Select ENSP00000349297.5:n.1183-164A>T
ENST00000322910.9:c.*1138-164A>T ENSP00000325395.5:n.*1138-164A>T
ENST00000350303.9:c.1117-164A>T ENSP00000344152.5:n.1117-164A>T
ENST00000356839.9:c.1183-164A>T ENSP00000349297.5:n.1183-164A>T
ENST00000542255.6:c.41-164A>T
ENST00000543245.6:c.1252-164A>T ENSP00000438689.2:n.1252-164A>T
ENST00000578579.2:n.190A>T
ENST00000578824.5:n.599-164A>T
ENST00000579425.5:n.207-164A>T
ENST00000579546.1:c.20-164A>T
ENST00000583858.5:c.212-164A>T
ENST00000585203.6:n.391-164A>T
NM_000018.3:c.1183-164A>T NP_000009.1:n.1183-164A>T
NM_001033859.2:c.1117-164A>T NP_001029031.1:n.1117-164A>T
NM_001270447.1:c.1252-164A>T NP_001257376.1:n.1252-164A>T
NM_001270448.1:c.955-164A>T NP_001257377.1:n.955-164A>T
XM_006721516.2:c.1183-164A>T XP_006721579.2:n.1183-164A>T
XM_011523829.1:c.1183-164A>T XP_011522131.1:n.1183-164A>T
XM_011523830.1:c.1183-164A>T XP_011522132.1:n.1183-164A>T
XR_934021.1:n.1290-164A>T
XR_934022.1:n.1290-164A>T
XR_934023.1:n.1290-164A>T
XM_006721516.3:c.1183-164A>T XP_006721579.2:n.1183-164A>T
XM_011523829.2:c.1183-164A>T XP_011522131.1:n.1183-164A>T
XM_011523830.2:c.1183-164A>T XP_011522132.1:n.1183-164A>T
XM_024450741.1:c.1183-164A>T XP_024306509.1:n.1183-164A>T
XR_934021.2:n.1242-164A>T
XR_934022.2:n.1242-164A>T
XR_934023.2:n.1242-164A>T
NM_000018.4:c.1183-164A>T MANE Select NP_000009.1:n.1183-164A>T
NM_001033859.3:c.1117-164A>T NP_001029031.1:n.1117-164A>T
NM_001270447.2:c.1252-164A>T NP_001257376.1:n.1252-164A>T
NM_001270448.2:c.955-164A>T NP_001257377.1:n.955-164A>T