Canonical Allele Identifier: CA397722064

Gene: ACADVL

Linked Data

• dbSNP Id: rs1247979958
• MyVariant Identifiers: chr17:g.7123464G>T (hg19) ; chr17:g.7220145G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220145G>T , CM000679.2:g.7220145G>T	GRCh38
NC_000017.10:g.7123464G>T , CM000679.1:g.7123464G>T	GRCh37
NC_000017.9:g.7064188G>T	NCBI36
NG_007975.1:g.5312G>T
NG_008391.2:g.4906C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.86G>T MANE Select	ENSP00000349297.5:p.Gly29Val
ENST00000322910.9:c.*41G>T	ENSP00000325395.5:n.*41G>T
ENST00000350303.9:c.86G>T	ENSP00000344152.5:p.Gly29Val
ENST00000356839.9:c.86G>T	ENSP00000349297.5:p.Gly29Val
ENST00000543245.6:c.155G>T	ENSP00000438689.2:p.Gly52Val
ENST00000577191.5:n.163G>T
ENST00000577857.5:n.176G>T
ENST00000578269.5:n.193G>T
ENST00000578421.1:n.220G>T
ENST00000579286.5:n.193G>T
ENST00000579886.2:c.86G>T	ENSP00000463246.1:p.Gly29Val
ENST00000580263.5:n.176G>T
ENST00000581562.5:n.133G>T
ENST00000582056.5:n.176G>T
ENST00000582356.5:n.211G>T
ENST00000583312.5:c.86G>T	ENSP00000467920.1:p.Gly29Val
ENST00000584103.5:c.86G>T	ENSP00000465353.1:p.Gly29Val
NM_000018.3:c.86G>T	NP_000009.1:p.Gly29Val
NM_001033859.2:c.86G>T	NP_001029031.1:p.Gly29Val
NM_001270447.1:c.155G>T	NP_001257376.1:p.Gly52Val
NM_001270448.1:c.-143G>T	NP_001257377.1:n.-143G>T
XM_006721516.2:c.86G>T	XP_006721579.2:p.Gly29Val
XM_011523829.1:c.86G>T	XP_011522131.1:p.Gly29Val
XM_011523830.1:c.86G>T	XP_011522132.1:p.Gly29Val
XR_934021.1:n.193G>T
XR_934022.1:n.193G>T
XR_934023.1:n.193G>T
XM_006721516.3:c.86G>T	XP_006721579.2:p.Gly29Val
XM_011523829.2:c.86G>T	XP_011522131.1:p.Gly29Val
XM_011523830.2:c.86G>T	XP_011522132.1:p.Gly29Val
XM_024450741.1:c.86G>T	XP_024306509.1:p.Gly29Val
XR_934021.2:n.145G>T
XR_934022.2:n.145G>T
XR_934023.2:n.145G>T
NM_000018.4:c.86G>T MANE Select	NP_000009.1:p.Gly29Val
NM_001033859.3:c.86G>T	NP_001029031.1:p.Gly29Val
NM_001270447.2:c.155G>T	NP_001257376.1:p.Gly52Val
NM_001270448.2:c.-143G>T	NP_001257377.1:n.-143G>T