Canonical Allele Identifier: CA397723154

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124935T>A (hg19) ; chr17:g.7221616T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221616T>A , CM000679.2:g.7221616T>A	GRCh38
NC_000017.10:g.7124935T>A , CM000679.1:g.7124935T>A	GRCh37
NC_000017.9:g.7065659T>A	NCBI36
NG_007975.1:g.6783T>A
NG_008391.2:g.3435A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.556T>A MANE Select	ENSP00000349297.5:p.Phe186Ile
ENST00000322910.9:c.*511T>A	ENSP00000325395.5:n.*511T>A
ENST00000350303.9:c.490T>A	ENSP00000344152.5:p.Phe164Ile
ENST00000356839.9:c.556T>A	ENSP00000349297.5:p.Phe186Ile
ENST00000543245.6:c.625T>A	ENSP00000438689.2:p.Phe209Ile
ENST00000577191.5:n.633T>A
ENST00000577433.5:n.764T>A
ENST00000577857.5:n.372T>A
ENST00000579286.5:n.737T>A
ENST00000579886.2:c.394T>A	ENSP00000463246.1:p.Phe132Ile
ENST00000580365.1:n.287T>A
ENST00000581378.5:c.274T>A
ENST00000581562.5:n.525-336T>A
ENST00000582166.1:n.537T>A
ENST00000583312.5:c.556T>A	ENSP00000467920.1:p.Phe186Ile
ENST00000583760.1:n.338T>A
NM_000018.3:c.556T>A	NP_000009.1:p.Phe186Ile
NM_001033859.2:c.490T>A	NP_001029031.1:p.Phe164Ile
NM_001270447.1:c.625T>A	NP_001257376.1:p.Phe209Ile
NM_001270448.1:c.328T>A	NP_001257377.1:p.Phe110Ile
XM_006721516.2:c.556T>A	XP_006721579.2:p.Phe186Ile
XM_011523829.1:c.556T>A	XP_011522131.1:p.Phe186Ile
XM_011523830.1:c.556T>A	XP_011522132.1:p.Phe186Ile
XR_934021.1:n.663T>A
XR_934022.1:n.663T>A
XR_934023.1:n.663T>A
XM_006721516.3:c.556T>A	XP_006721579.2:p.Phe186Ile
XM_011523829.2:c.556T>A	XP_011522131.1:p.Phe186Ile
XM_011523830.2:c.556T>A	XP_011522132.1:p.Phe186Ile
XM_024450741.1:c.556T>A	XP_024306509.1:p.Phe186Ile
XR_934021.2:n.615T>A
XR_934022.2:n.615T>A
XR_934023.2:n.615T>A
NM_000018.4:c.556T>A MANE Select	NP_000009.1:p.Phe186Ile
NM_001033859.3:c.490T>A	NP_001029031.1:p.Phe164Ile
NM_001270447.2:c.625T>A	NP_001257376.1:p.Phe209Ile
NM_001270448.2:c.328T>A	NP_001257377.1:p.Phe110Ile