Canonical Allele Identifier: CA397723182

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124947C>A (hg19) ; chr17:g.7221628C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221628C>A , CM000679.2:g.7221628C>A	GRCh38
NC_000017.10:g.7124947C>A , CM000679.1:g.7124947C>A	GRCh37
NC_000017.9:g.7065671C>A	NCBI36
NG_007975.1:g.6795C>A
NG_008391.2:g.3423G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.568C>A MANE Select	ENSP00000349297.5:p.Leu190Met
ENST00000322910.9:c.*523C>A	ENSP00000325395.5:n.*523C>A
ENST00000350303.9:c.502C>A	ENSP00000344152.5:p.Leu168Met
ENST00000356839.9:c.568C>A	ENSP00000349297.5:p.Leu190Met
ENST00000543245.6:c.637C>A	ENSP00000438689.2:p.Leu213Met
ENST00000577191.5:n.645C>A
ENST00000577433.5:n.776C>A
ENST00000577857.5:n.384C>A
ENST00000579286.5:n.749C>A
ENST00000579886.2:c.406C>A	ENSP00000463246.1:p.Leu136Met
ENST00000580365.1:n.299C>A
ENST00000581378.5:c.286C>A
ENST00000581562.5:n.525-324C>A
ENST00000582166.1:n.549C>A
ENST00000583312.5:c.568C>A	ENSP00000467920.1:p.Leu190Met
ENST00000583760.1:n.350C>A
NM_000018.3:c.568C>A	NP_000009.1:p.Leu190Met
NM_001033859.2:c.502C>A	NP_001029031.1:p.Leu168Met
NM_001270447.1:c.637C>A	NP_001257376.1:p.Leu213Met
NM_001270448.1:c.340C>A	NP_001257377.1:p.Leu114Met
XM_006721516.2:c.568C>A	XP_006721579.2:p.Leu190Met
XM_011523829.1:c.568C>A	XP_011522131.1:p.Leu190Met
XM_011523830.1:c.568C>A	XP_011522132.1:p.Leu190Met
XR_934021.1:n.675C>A
XR_934022.1:n.675C>A
XR_934023.1:n.675C>A
XM_006721516.3:c.568C>A	XP_006721579.2:p.Leu190Met
XM_011523829.2:c.568C>A	XP_011522131.1:p.Leu190Met
XM_011523830.2:c.568C>A	XP_011522132.1:p.Leu190Met
XM_024450741.1:c.568C>A	XP_024306509.1:p.Leu190Met
XR_934021.2:n.627C>A
XR_934022.2:n.627C>A
XR_934023.2:n.627C>A
NM_000018.4:c.568C>A MANE Select	NP_000009.1:p.Leu190Met
NM_001033859.3:c.502C>A	NP_001029031.1:p.Leu168Met
NM_001270447.2:c.637C>A	NP_001257376.1:p.Leu213Met
NM_001270448.2:c.340C>A	NP_001257377.1:p.Leu114Met