Canonical Allele Identifier: CA397723411

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7125307C>A (hg19) ; chr17:g.7221988C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221988C>A , CM000679.2:g.7221988C>A	GRCh38
NC_000017.10:g.7125307C>A , CM000679.1:g.7125307C>A	GRCh37
NC_000017.9:g.7066031C>A	NCBI36
NG_007975.1:g.7155C>A
NG_008391.2:g.3063G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.659C>A MANE Select	ENSP00000349297.5:p.Ser220Ter
ENST00000322910.9:c.*614C>A	ENSP00000325395.5:n.*614C>A
ENST00000350303.9:c.593C>A	ENSP00000344152.5:p.Ser198Ter
ENST00000356839.9:c.659C>A	ENSP00000349297.5:p.Ser220Ter
ENST00000543245.6:c.728C>A	ENSP00000438689.2:p.Ser243Ter
ENST00000577191.5:n.736C>A
ENST00000577857.5:n.475C>A
ENST00000579286.5:n.840C>A
ENST00000580365.1:n.390C>A
ENST00000581378.5:c.377C>A
ENST00000581562.5:n.561C>A
ENST00000582379.1:n.43C>A
ENST00000583312.5:c.674C>A
ENST00000583760.1:n.441C>A
NM_000018.3:c.659C>A	NP_000009.1:p.Ser220Ter
NM_001033859.2:c.593C>A	NP_001029031.1:p.Ser198Ter
NM_001270447.1:c.728C>A	NP_001257376.1:p.Ser243Ter
NM_001270448.1:c.431C>A	NP_001257377.1:p.Ser144Ter
XM_006721516.2:c.659C>A	XP_006721579.2:p.Ser220Ter
XM_011523829.1:c.659C>A	XP_011522131.1:p.Ser220Ter
XM_011523830.1:c.659C>A	XP_011522132.1:p.Ser220Ter
XR_934021.1:n.766C>A
XR_934022.1:n.766C>A
XR_934023.1:n.766C>A
XM_006721516.3:c.659C>A	XP_006721579.2:p.Ser220Ter
XM_011523829.2:c.659C>A	XP_011522131.1:p.Ser220Ter
XM_011523830.2:c.659C>A	XP_011522132.1:p.Ser220Ter
XM_024450741.1:c.659C>A	XP_024306509.1:p.Ser220Ter
XR_934021.2:n.718C>A
XR_934022.2:n.718C>A
XR_934023.2:n.718C>A
NM_000018.4:c.659C>A MANE Select	NP_000009.1:p.Ser220Ter
NM_001033859.3:c.593C>A	NP_001029031.1:p.Ser198Ter
NM_001270447.2:c.728C>A	NP_001257376.1:p.Ser243Ter
NM_001270448.2:c.431C>A	NP_001257377.1:p.Ser144Ter