Canonical Allele Identifier: CA497693909

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124353T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221034T>G , CM000679.2:g.7221034T>G	GRCh38
NC_000017.10:g.7124353T>G , CM000679.1:g.7124353T>G	GRCh37
NC_000017.9:g.7065077T>G	NCBI36
NG_007975.1:g.6201T>G
NG_008391.2:g.4017A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.453T>G MANE Select	ENSP00000349297.5:p.Gly151=
ENST00000322910.9:c.*408T>G	ENSP00000325395.5:n.*408T>G
ENST00000350303.9:c.387T>G	ENSP00000344152.5:p.Gly129=
ENST00000356839.9:c.453T>G	ENSP00000349297.5:p.Gly151=
ENST00000543245.6:c.522T>G	ENSP00000438689.2:p.Gly174=
ENST00000577191.5:n.530T>G
ENST00000577433.5:n.661T>G
ENST00000577857.5:n.293+204T>G
ENST00000579286.5:n.634T>G
ENST00000579886.2:c.291T>G	ENSP00000463246.1:p.Gly97=
ENST00000580365.1:n.184T>G
ENST00000581378.5:c.152T>G
ENST00000581562.5:n.500T>G
ENST00000582056.5:n.636T>G
ENST00000582166.1:n.434T>G
ENST00000583312.5:c.453T>G	ENSP00000467920.1:p.Gly151=
NM_000018.3:c.453T>G	NP_000009.1:p.Gly151=
NM_001033859.2:c.387T>G	NP_001029031.1:p.Gly129=
NM_001270447.1:c.522T>G	NP_001257376.1:p.Gly174=
NM_001270448.1:c.225T>G	NP_001257377.1:p.Gly75=
XM_006721516.2:c.453T>G	XP_006721579.2:p.Gly151=
XM_011523829.1:c.453T>G	XP_011522131.1:p.Gly151=
XM_011523830.1:c.453T>G	XP_011522132.1:p.Gly151=
XR_934021.1:n.560T>G
XR_934022.1:n.560T>G
XR_934023.1:n.560T>G
XM_006721516.3:c.453T>G	XP_006721579.2:p.Gly151=
XM_011523829.2:c.453T>G	XP_011522131.1:p.Gly151=
XM_011523830.2:c.453T>G	XP_011522132.1:p.Gly151=
XM_024450741.1:c.453T>G	XP_024306509.1:p.Gly151=
XR_934021.2:n.512T>G
XR_934022.2:n.512T>G
XR_934023.2:n.512T>G
NM_000018.4:c.453T>G MANE Select	NP_000009.1:p.Gly151=
NM_001033859.3:c.387T>G	NP_001029031.1:p.Gly129=
NM_001270447.2:c.522T>G	NP_001257376.1:p.Gly174=
NM_001270448.2:c.225T>G	NP_001257377.1:p.Gly75=