Canonical Allele Identifier: CA397724813

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127162A>G (hg19) ; chr17:g.7223843A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223843A>G , CM000679.2:g.7223843A>G	GRCh38
NC_000017.10:g.7127162A>G , CM000679.1:g.7127162A>G	GRCh37
NC_000017.9:g.7067886A>G	NCBI36
NG_007975.1:g.9010A>G
NG_008391.2:g.1208T>C
NG_033038.1:g.15702T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1300A>G MANE Select	ENSP00000349297.5:p.Ile434Val
ENST00000322910.9:c.*1255A>G	ENSP00000325395.5:n.*1255A>G
ENST00000350303.9:c.1234A>G	ENSP00000344152.5:p.Ile412Val
ENST00000356839.9:c.1300A>G	ENSP00000349297.5:p.Ile434Val
ENST00000542255.6:c.158A>G
ENST00000543245.6:c.1369A>G	ENSP00000438689.2:p.Ile457Val
ENST00000578711.1:n.339A>G
ENST00000578824.5:n.716A>G
ENST00000579425.5:n.324A>G
ENST00000579546.1:c.137A>G
ENST00000583074.5:n.19A>G
ENST00000583850.5:n.75A>G
ENST00000583858.5:c.329A>G
ENST00000585203.6:n.508A>G
NM_000018.3:c.1300A>G	NP_000009.1:p.Ile434Val
NM_001033859.2:c.1234A>G	NP_001029031.1:p.Ile412Val
NM_001270447.1:c.1369A>G	NP_001257376.1:p.Ile457Val
NM_001270448.1:c.1072A>G	NP_001257377.1:p.Ile358Val
XM_006721516.2:c.1300A>G	XP_006721579.2:p.Ile434Val
XM_011523829.1:c.1300A>G	XP_011522131.1:p.Ile434Val
XM_011523830.1:c.1300A>G	XP_011522132.1:p.Ile434Val
XR_934021.1:n.1407A>G
XR_934022.1:n.1407A>G
XR_934023.1:n.1407A>G
XM_006721516.3:c.1300A>G	XP_006721579.2:p.Ile434Val
XM_011523829.2:c.1300A>G	XP_011522131.1:p.Ile434Val
XM_011523830.2:c.1300A>G	XP_011522132.1:p.Ile434Val
XM_024450741.1:c.1300A>G	XP_024306509.1:p.Ile434Val
XR_934021.2:n.1359A>G
XR_934022.2:n.1359A>G
XR_934023.2:n.1359A>G
NM_000018.4:c.1300A>G MANE Select	NP_000009.1:p.Ile434Val
NM_001033859.3:c.1234A>G	NP_001029031.1:p.Ile412Val
NM_001270447.2:c.1369A>G	NP_001257376.1:p.Ile457Val
NM_001270448.2:c.1072A>G	NP_001257377.1:p.Ile358Val