Canonical Allele Identifier: CA497620640

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7126469T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223150T>C , CM000679.2:g.7223150T>C	GRCh38
NC_000017.10:g.7126469T>C , CM000679.1:g.7126469T>C	GRCh37
NC_000017.9:g.7067193T>C	NCBI36
NG_007975.1:g.8317T>C
NG_008391.2:g.1901A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1095T>C MANE Select	ENSP00000349297.5:p.Asn365=
ENST00000322910.9:c.*1050T>C	ENSP00000325395.5:n.*1050T>C
ENST00000350303.9:c.1029T>C	ENSP00000344152.5:p.Asn343=
ENST00000356839.9:c.1095T>C	ENSP00000349297.5:p.Asn365=
ENST00000543245.6:c.1164T>C	ENSP00000438689.2:p.Asn388=
ENST00000578579.2:n.44T>C
ENST00000578824.5:n.511T>C
ENST00000579425.5:n.119T>C
ENST00000582379.1:n.746T>C
ENST00000583858.5:c.124T>C
ENST00000585203.6:n.303T>C
NM_000018.3:c.1095T>C	NP_000009.1:p.Asn365=
NM_001033859.2:c.1029T>C	NP_001029031.1:p.Asn343=
NM_001270447.1:c.1164T>C	NP_001257376.1:p.Asn388=
NM_001270448.1:c.867T>C	NP_001257377.1:p.Asn289=
XM_006721516.2:c.1095T>C	XP_006721579.2:p.Asn365=
XM_011523829.1:c.1095T>C	XP_011522131.1:p.Asn365=
XM_011523830.1:c.1095T>C	XP_011522132.1:p.Asn365=
XR_934021.1:n.1202T>C
XR_934022.1:n.1202T>C
XR_934023.1:n.1202T>C
XM_006721516.3:c.1095T>C	XP_006721579.2:p.Asn365=
XM_011523829.2:c.1095T>C	XP_011522131.1:p.Asn365=
XM_011523830.2:c.1095T>C	XP_011522132.1:p.Asn365=
XM_024450741.1:c.1095T>C	XP_024306509.1:p.Asn365=
XR_934021.2:n.1154T>C
XR_934022.2:n.1154T>C
XR_934023.2:n.1154T>C
NM_000018.4:c.1095T>C MANE Select	NP_000009.1:p.Asn365=
NM_001033859.3:c.1029T>C	NP_001029031.1:p.Asn343=
NM_001270447.2:c.1164T>C	NP_001257376.1:p.Asn388=
NM_001270448.2:c.867T>C	NP_001257377.1:p.Asn289=