Canonical Allele Identifier: CA497620228

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7126085T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222766T>G , CM000679.2:g.7222766T>G	GRCh38
NC_000017.10:g.7126085T>G , CM000679.1:g.7126085T>G	GRCh37
NC_000017.9:g.7066809T>G	NCBI36
NG_007975.1:g.7933T>G
NG_008391.2:g.2285A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.978T>G MANE Select	ENSP00000349297.5:p.Val326=
ENST00000322910.9:c.*933T>G	ENSP00000325395.5:n.*933T>G
ENST00000350303.9:c.912T>G	ENSP00000344152.5:p.Val304=
ENST00000356839.9:c.978T>G	ENSP00000349297.5:p.Val326=
ENST00000543245.6:c.1047T>G	ENSP00000438689.2:p.Val349=
ENST00000578824.5:n.127T>G
ENST00000581378.5:c.696T>G
ENST00000582379.1:n.362T>G
ENST00000583858.5:c.7T>G
NM_000018.3:c.978T>G	NP_000009.1:p.Val326=
NM_001033859.2:c.912T>G	NP_001029031.1:p.Val304=
NM_001270447.1:c.1047T>G	NP_001257376.1:p.Val349=
NM_001270448.1:c.750T>G	NP_001257377.1:p.Val250=
XM_006721516.2:c.978T>G	XP_006721579.2:p.Val326=
XM_011523829.1:c.978T>G	XP_011522131.1:p.Val326=
XM_011523830.1:c.978T>G	XP_011522132.1:p.Val326=
XR_934021.1:n.1085T>G
XR_934022.1:n.1085T>G
XR_934023.1:n.1085T>G
XM_006721516.3:c.978T>G	XP_006721579.2:p.Val326=
XM_011523829.2:c.978T>G	XP_011522131.1:p.Val326=
XM_011523830.2:c.978T>G	XP_011522132.1:p.Val326=
XM_024450741.1:c.978T>G	XP_024306509.1:p.Val326=
XR_934021.2:n.1037T>G
XR_934022.2:n.1037T>G
XR_934023.2:n.1037T>G
NM_000018.4:c.978T>G MANE Select	NP_000009.1:p.Val326=
NM_001033859.3:c.912T>G	NP_001029031.1:p.Val304=
NM_001270447.2:c.1047T>G	NP_001257376.1:p.Val349=
NM_001270448.2:c.750T>G	NP_001257377.1:p.Val250=