Canonical Allele Identifier: CA397725089

Gene: ACADVL

Linked Data

• dbSNP Id: rs2071357482
• MyVariant Identifiers: chr17:g.7127381G>T (hg19) ; chr17:g.7224062G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224062G>T , CM000679.2:g.7224062G>T	GRCh38
NC_000017.10:g.7127381G>T , CM000679.1:g.7127381G>T	GRCh37
NC_000017.9:g.7068105G>T	NCBI36
NG_007975.1:g.9229G>T
NG_008391.2:g.989C>A
NG_033038.1:g.15483C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1427G>T MANE Select	ENSP00000349297.5:p.Gly476Val
ENST00000322910.9:c.*1382G>T	ENSP00000325395.5:n.*1382G>T
ENST00000350303.9:c.1361G>T	ENSP00000344152.5:p.Gly454Val
ENST00000356839.9:c.1427G>T	ENSP00000349297.5:p.Gly476Val
ENST00000542255.6:c.285G>T
ENST00000543245.6:c.1496G>T	ENSP00000438689.2:p.Gly499Val
ENST00000578711.1:n.558G>T
ENST00000579425.5:n.543G>T
ENST00000579546.1:c.264G>T
ENST00000579894.5:n.138G>T
ENST00000583074.5:n.146G>T
ENST00000583850.5:n.202G>T
ENST00000583858.5:c.456G>T
ENST00000585203.6:n.618G>T
NM_000018.3:c.1427G>T	NP_000009.1:p.Gly476Val
NM_001033859.2:c.1361G>T	NP_001029031.1:p.Gly454Val
NM_001270447.1:c.1496G>T	NP_001257376.1:p.Gly499Val
NM_001270448.1:c.1199G>T	NP_001257377.1:p.Gly400Val
XM_006721516.2:c.1427G>T	XP_006721579.2:p.Gly476Val
XM_011523829.1:c.1427G>T	XP_011522131.1:p.Gly476Val
XM_011523830.1:c.1427G>T	XP_011522132.1:p.Gly476Val
XR_934021.1:n.1534G>T
XR_934022.1:n.1534G>T
XR_934023.1:n.1534G>T
XM_006721516.3:c.1427G>T	XP_006721579.2:p.Gly476Val
XM_011523829.2:c.1427G>T	XP_011522131.1:p.Gly476Val
XM_011523830.2:c.1427G>T	XP_011522132.1:p.Gly476Val
XM_024450741.1:c.1427G>T	XP_024306509.1:p.Gly476Val
XR_934021.2:n.1486G>T
XR_934022.2:n.1486G>T
XR_934023.2:n.1486G>T
NM_000018.4:c.1427G>T MANE Select	NP_000009.1:p.Gly476Val
NM_001033859.3:c.1361G>T	NP_001029031.1:p.Gly454Val
NM_001270447.2:c.1496G>T	NP_001257376.1:p.Gly499Val
NM_001270448.2:c.1199G>T	NP_001257377.1:p.Gly400Val