Canonical Allele Identifier: CA497694413

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127962T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224643T>C , CM000679.2:g.7224643T>C	GRCh38
NC_000017.10:g.7127962T>C , CM000679.1:g.7127962T>C	GRCh37
NC_000017.9:g.7068686T>C	NCBI36
NG_007975.1:g.9810T>C
NG_008391.2:g.408A>G
NG_033038.1:g.14902A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1680T>C MANE Select	ENSP00000349297.5:p.Asn560=
ENST00000322910.9:c.*1635T>C	ENSP00000325395.5:n.*1635T>C
ENST00000350303.9:c.1614T>C	ENSP00000344152.5:p.Asn538=
ENST00000356839.9:c.1680T>C	ENSP00000349297.5:p.Asn560=
ENST00000542255.6:c.537-72T>C
ENST00000543245.6:c.1749T>C	ENSP00000438689.2:p.Asn583=
ENST00000578033.1:n.11T>C
ENST00000578319.5:n.261T>C
ENST00000578711.1:n.1139T>C
ENST00000578809.5:n.252T>C
ENST00000579425.5:n.796T>C
ENST00000579546.1:c.415T>C
ENST00000582450.1:n.277T>C
ENST00000583074.5:n.300-72T>C
ENST00000583848.5:c.65-19T>C	ENSP00000466487.1:n.65-19T>C
ENST00000583850.5:n.451T>C
ENST00000583858.5:c.611T>C
ENST00000585203.6:n.871T>C
NM_000018.3:c.1680T>C	NP_000009.1:p.Asn560=
NM_001033859.2:c.1614T>C	NP_001029031.1:p.Asn538=
NM_001270447.1:c.1749T>C	NP_001257376.1:p.Asn583=
NM_001270448.1:c.1452T>C	NP_001257377.1:p.Asn484=
XM_006721516.2:c.1679-72T>C	XP_006721579.2:n.1679-72T>C
XM_011523829.1:c.1577-72T>C	XP_011522131.1:n.1577-72T>C
XM_011523830.1:c.1578T>C	XP_011522132.1:p.Asn526=
XR_934021.1:n.1783T>C
XR_934022.1:n.1689T>C
XR_934023.1:n.1688-72T>C
XM_006721516.3:c.1679-72T>C	XP_006721579.2:n.1679-72T>C
XM_011523829.2:c.1577-72T>C	XP_011522131.1:n.1577-72T>C
XM_011523830.2:c.1578T>C	XP_011522132.1:p.Asn526=
XM_024450741.1:c.1668T>C	XP_024306509.1:p.Asn556=
XR_934021.2:n.1735T>C
XR_934022.2:n.1641T>C
XR_934023.2:n.1640-72T>C
NM_000018.4:c.1680T>C MANE Select	NP_000009.1:p.Asn560=
NM_001033859.3:c.1614T>C	NP_001029031.1:p.Asn538=
NM_001270447.2:c.1749T>C	NP_001257376.1:p.Asn583=
NM_001270448.2:c.1452T>C	NP_001257377.1:p.Asn484=