Canonical Allele Identifier: CA397723396

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7125301A>T (hg19) ; chr17:g.7221982A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221982A>T , CM000679.2:g.7221982A>T	GRCh38
NC_000017.10:g.7125301A>T , CM000679.1:g.7125301A>T	GRCh37
NC_000017.9:g.7066025A>T	NCBI36
NG_007975.1:g.7149A>T
NG_008391.2:g.3069T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.653A>T MANE Select	ENSP00000349297.5:p.Glu218Val
ENST00000322910.9:c.*608A>T	ENSP00000325395.5:n.*608A>T
ENST00000350303.9:c.587A>T	ENSP00000344152.5:p.Glu196Val
ENST00000356839.9:c.653A>T	ENSP00000349297.5:p.Glu218Val
ENST00000543245.6:c.722A>T	ENSP00000438689.2:p.Glu241Val
ENST00000577191.5:n.730A>T
ENST00000577857.5:n.469A>T
ENST00000579286.5:n.834A>T
ENST00000580365.1:n.384A>T
ENST00000581378.5:c.371A>T
ENST00000581562.5:n.555A>T
ENST00000582379.1:n.37A>T
ENST00000583312.5:c.668A>T	ENSP00000467920.1:p.Glu223Val
ENST00000583760.1:n.435A>T
NM_000018.3:c.653A>T	NP_000009.1:p.Glu218Val
NM_001033859.2:c.587A>T	NP_001029031.1:p.Glu196Val
NM_001270447.1:c.722A>T	NP_001257376.1:p.Glu241Val
NM_001270448.1:c.425A>T	NP_001257377.1:p.Glu142Val
XM_006721516.2:c.653A>T	XP_006721579.2:p.Glu218Val
XM_011523829.1:c.653A>T	XP_011522131.1:p.Glu218Val
XM_011523830.1:c.653A>T	XP_011522132.1:p.Glu218Val
XR_934021.1:n.760A>T
XR_934022.1:n.760A>T
XR_934023.1:n.760A>T
XM_006721516.3:c.653A>T	XP_006721579.2:p.Glu218Val
XM_011523829.2:c.653A>T	XP_011522131.1:p.Glu218Val
XM_011523830.2:c.653A>T	XP_011522132.1:p.Glu218Val
XM_024450741.1:c.653A>T	XP_024306509.1:p.Glu218Val
XR_934021.2:n.712A>T
XR_934022.2:n.712A>T
XR_934023.2:n.712A>T
NM_000018.4:c.653A>T MANE Select	NP_000009.1:p.Glu218Val
NM_001033859.3:c.587A>T	NP_001029031.1:p.Glu196Val
NM_001270447.2:c.722A>T	NP_001257376.1:p.Glu241Val
NM_001270448.2:c.425A>T	NP_001257377.1:p.Glu142Val