Canonical Allele Identifier: CA397724130

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7126105C>A (hg19) ; chr17:g.7222786C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222786C>A , CM000679.2:g.7222786C>A	GRCh38
NC_000017.10:g.7126105C>A , CM000679.1:g.7126105C>A	GRCh37
NC_000017.9:g.7066829C>A	NCBI36
NG_007975.1:g.7953C>A
NG_008391.2:g.2265G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.998C>A MANE Select	ENSP00000349297.5:p.Ala333Asp
ENST00000322910.9:c.*953C>A	ENSP00000325395.5:n.*953C>A
ENST00000350303.9:c.932C>A	ENSP00000344152.5:p.Ala311Asp
ENST00000356839.9:c.998C>A	ENSP00000349297.5:p.Ala333Asp
ENST00000543245.6:c.1067C>A	ENSP00000438689.2:p.Ala356Asp
ENST00000578824.5:n.147C>A
ENST00000581378.5:c.716C>A
ENST00000582379.1:n.382C>A
ENST00000583858.5:c.27C>A
NM_000018.3:c.998C>A	NP_000009.1:p.Ala333Asp
NM_001033859.2:c.932C>A	NP_001029031.1:p.Ala311Asp
NM_001270447.1:c.1067C>A	NP_001257376.1:p.Ala356Asp
NM_001270448.1:c.770C>A	NP_001257377.1:p.Ala257Asp
XM_006721516.2:c.998C>A	XP_006721579.2:p.Ala333Asp
XM_011523829.1:c.998C>A	XP_011522131.1:p.Ala333Asp
XM_011523830.1:c.998C>A	XP_011522132.1:p.Ala333Asp
XR_934021.1:n.1105C>A
XR_934022.1:n.1105C>A
XR_934023.1:n.1105C>A
XM_006721516.3:c.998C>A	XP_006721579.2:p.Ala333Asp
XM_011523829.2:c.998C>A	XP_011522131.1:p.Ala333Asp
XM_011523830.2:c.998C>A	XP_011522132.1:p.Ala333Asp
XM_024450741.1:c.998C>A	XP_024306509.1:p.Ala333Asp
XR_934021.2:n.1057C>A
XR_934022.2:n.1057C>A
XR_934023.2:n.1057C>A
NM_000018.4:c.998C>A MANE Select	NP_000009.1:p.Ala333Asp
NM_001033859.3:c.932C>A	NP_001029031.1:p.Ala311Asp
NM_001270447.2:c.1067C>A	NP_001257376.1:p.Ala356Asp
NM_001270448.2:c.770C>A	NP_001257377.1:p.Ala257Asp