Canonical Allele Identifier: CA2635781455

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7221834-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221834A>G , CM000679.2:g.7221834A>G	GRCh38
NC_000017.10:g.7125153A>G , CM000679.1:g.7125153A>G	GRCh37
NC_000017.9:g.7065877A>G	NCBI36
NG_007975.1:g.7001A>G
NG_008391.2:g.3217T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.623-118A>G MANE Select	ENSP00000349297.5:n.623-118A>G
ENST00000322910.9:c.*578-118A>G	ENSP00000325395.5:n.*578-118A>G
ENST00000350303.9:c.557-118A>G	ENSP00000344152.5:n.557-118A>G
ENST00000356839.9:c.623-118A>G	ENSP00000349297.5:n.623-118A>G
ENST00000543245.6:c.692-118A>G	ENSP00000438689.2:n.692-118A>G
ENST00000577191.5:n.700-118A>G
ENST00000577857.5:n.439-118A>G
ENST00000579286.5:n.804-118A>G
ENST00000579886.2:c.461-118A>G	ENSP00000463246.1:n.461-118A>G
ENST00000580365.1:n.354-118A>G
ENST00000581378.5:c.341-118A>G
ENST00000581562.5:n.525-118A>G
ENST00000583312.5:c.623-103A>G	ENSP00000467920.1:n.623-103A>G
ENST00000583760.1:n.405-118A>G
NM_000018.3:c.623-118A>G	NP_000009.1:n.623-118A>G
NM_001033859.2:c.557-118A>G	NP_001029031.1:n.557-118A>G
NM_001270447.1:c.692-118A>G	NP_001257376.1:n.692-118A>G
NM_001270448.1:c.395-118A>G	NP_001257377.1:n.395-118A>G
XM_006721516.2:c.623-118A>G	XP_006721579.2:n.623-118A>G
XM_011523829.1:c.623-118A>G	XP_011522131.1:n.623-118A>G
XM_011523830.1:c.623-118A>G	XP_011522132.1:n.623-118A>G
XR_934021.1:n.730-118A>G
XR_934022.1:n.730-118A>G
XR_934023.1:n.730-118A>G
XM_006721516.3:c.623-118A>G	XP_006721579.2:n.623-118A>G
XM_011523829.2:c.623-118A>G	XP_011522131.1:n.623-118A>G
XM_011523830.2:c.623-118A>G	XP_011522132.1:n.623-118A>G
XM_024450741.1:c.623-118A>G	XP_024306509.1:n.623-118A>G
XR_934021.2:n.682-118A>G
XR_934022.2:n.682-118A>G
XR_934023.2:n.682-118A>G
NM_000018.4:c.623-118A>G MANE Select	NP_000009.1:n.623-118A>G
NM_001033859.3:c.557-118A>G	NP_001029031.1:n.557-118A>G
NM_001270447.2:c.692-118A>G	NP_001257376.1:n.692-118A>G
NM_001270448.2:c.395-118A>G	NP_001257377.1:n.395-118A>G