Canonical Allele Identifier: CA2635781809

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7222102-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222102C>G , CM000679.2:g.7222102C>G	GRCh38
NC_000017.10:g.7125421C>G , CM000679.1:g.7125421C>G	GRCh37
NC_000017.9:g.7066145C>G	NCBI36
NG_007975.1:g.7269C>G
NG_008391.2:g.2949G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.752+21C>G MANE Select	ENSP00000349297.5:n.752+21C>G
ENST00000322910.9:c.*707+21C>G	ENSP00000325395.5:n.*707+21C>G
ENST00000350303.9:c.686+21C>G	ENSP00000344152.5:n.686+21C>G
ENST00000356839.9:c.752+21C>G	ENSP00000349297.5:n.752+21C>G
ENST00000543245.6:c.821+21C>G	ENSP00000438689.2:n.821+21C>G
ENST00000577191.5:n.850C>G
ENST00000581378.5:c.470+21C>G
ENST00000582379.1:n.136+21C>G
ENST00000583760.1:n.555C>G
NM_000018.3:c.752+21C>G	NP_000009.1:n.752+21C>G
NM_001033859.2:c.686+21C>G	NP_001029031.1:n.686+21C>G
NM_001270447.1:c.821+21C>G	NP_001257376.1:n.821+21C>G
NM_001270448.1:c.524+21C>G	NP_001257377.1:n.524+21C>G
XM_006721516.2:c.752+21C>G	XP_006721579.2:n.752+21C>G
XM_011523829.1:c.752+21C>G	XP_011522131.1:n.752+21C>G
XM_011523830.1:c.752+21C>G	XP_011522132.1:n.752+21C>G
XR_934021.1:n.859+21C>G
XR_934022.1:n.859+21C>G
XR_934023.1:n.859+21C>G
XM_006721516.3:c.752+21C>G	XP_006721579.2:n.752+21C>G
XM_011523829.2:c.752+21C>G	XP_011522131.1:n.752+21C>G
XM_011523830.2:c.752+21C>G	XP_011522132.1:n.752+21C>G
XM_024450741.1:c.752+21C>G	XP_024306509.1:n.752+21C>G
XR_934021.2:n.811+21C>G
XR_934022.2:n.811+21C>G
XR_934023.2:n.811+21C>G
NM_000018.4:c.752+21C>G MANE Select	NP_000009.1:n.752+21C>G
NM_001033859.3:c.686+21C>G	NP_001029031.1:n.686+21C>G
NM_001270447.2:c.821+21C>G	NP_001257376.1:n.821+21C>G
NM_001270448.2:c.524+21C>G	NP_001257377.1:n.524+21C>G