Canonical Allele Identifier: CA397724937

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127305G>T (hg19) ; chr17:g.7223986G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223986G>T , CM000679.2:g.7223986G>T	GRCh38
NC_000017.10:g.7127305G>T , CM000679.1:g.7127305G>T	GRCh37
NC_000017.9:g.7068029G>T	NCBI36
NG_007975.1:g.9153G>T
NG_008391.2:g.1065C>A
NG_033038.1:g.15559C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1351G>T MANE Select	ENSP00000349297.5:p.Val451Leu
ENST00000322910.9:c.*1306G>T	ENSP00000325395.5:n.*1306G>T
ENST00000350303.9:c.1285G>T	ENSP00000344152.5:p.Val429Leu
ENST00000356839.9:c.1351G>T	ENSP00000349297.5:p.Val451Leu
ENST00000542255.6:c.209G>T
ENST00000543245.6:c.1420G>T	ENSP00000438689.2:p.Val474Leu
ENST00000578711.1:n.482G>T
ENST00000579425.5:n.467G>T
ENST00000579546.1:c.188G>T
ENST00000579894.5:n.62G>T
ENST00000583074.5:n.70G>T
ENST00000583850.5:n.126G>T
ENST00000583858.5:c.380G>T
ENST00000585203.6:n.542G>T
NM_000018.3:c.1351G>T	NP_000009.1:p.Val451Leu
NM_001033859.2:c.1285G>T	NP_001029031.1:p.Val429Leu
NM_001270447.1:c.1420G>T	NP_001257376.1:p.Val474Leu
NM_001270448.1:c.1123G>T	NP_001257377.1:p.Val375Leu
XM_006721516.2:c.1351G>T	XP_006721579.2:p.Val451Leu
XM_011523829.1:c.1351G>T	XP_011522131.1:p.Val451Leu
XM_011523830.1:c.1351G>T	XP_011522132.1:p.Val451Leu
XR_934021.1:n.1458G>T
XR_934022.1:n.1458G>T
XR_934023.1:n.1458G>T
XM_006721516.3:c.1351G>T	XP_006721579.2:p.Val451Leu
XM_011523829.2:c.1351G>T	XP_011522131.1:p.Val451Leu
XM_011523830.2:c.1351G>T	XP_011522132.1:p.Val451Leu
XM_024450741.1:c.1351G>T	XP_024306509.1:p.Val451Leu
XR_934021.2:n.1410G>T
XR_934022.2:n.1410G>T
XR_934023.2:n.1410G>T
NM_000018.4:c.1351G>T MANE Select	NP_000009.1:p.Val451Leu
NM_001033859.3:c.1285G>T	NP_001029031.1:p.Val429Leu
NM_001270447.2:c.1420G>T	NP_001257376.1:p.Val474Leu
NM_001270448.2:c.1123G>T	NP_001257377.1:p.Val375Leu