Canonical Allele Identifier: CA397725009

Gene: ACADVL

Linked Data

• ClinVar Variation Id: 932771
• ClinVar RCV Id: RCV001200712
• dbSNP Id: rs2071355667
• MyVariant Identifiers: chr17:g.7127341G>C (hg19) ; chr17:g.7224022G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224022G>C , CM000679.2:g.7224022G>C	GRCh38
NC_000017.10:g.7127341G>C , CM000679.1:g.7127341G>C	GRCh37
NC_000017.9:g.7068065G>C	NCBI36
NG_007975.1:g.9189G>C
NG_008391.2:g.1029C>G
NG_033038.1:g.15523C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1387G>C MANE Select	ENSP00000349297.5:p.Gly463Arg
ENST00000322910.9:c.*1342G>C	ENSP00000325395.5:n.*1342G>C
ENST00000350303.9:c.1321G>C	ENSP00000344152.5:p.Gly441Arg
ENST00000356839.9:c.1387G>C	ENSP00000349297.5:p.Gly463Arg
ENST00000542255.6:c.245G>C
ENST00000543245.6:c.1456G>C	ENSP00000438689.2:p.Gly486Arg
ENST00000578711.1:n.518G>C
ENST00000579425.5:n.503G>C
ENST00000579546.1:c.224G>C
ENST00000579894.5:n.98G>C
ENST00000583074.5:n.106G>C
ENST00000583850.5:n.162G>C
ENST00000583858.5:c.416G>C
ENST00000585203.6:n.578G>C
NM_000018.3:c.1387G>C	NP_000009.1:p.Gly463Arg
NM_001033859.2:c.1321G>C	NP_001029031.1:p.Gly441Arg
NM_001270447.1:c.1456G>C	NP_001257376.1:p.Gly486Arg
NM_001270448.1:c.1159G>C	NP_001257377.1:p.Gly387Arg
XM_006721516.2:c.1387G>C	XP_006721579.2:p.Gly463Arg
XM_011523829.1:c.1387G>C	XP_011522131.1:p.Gly463Arg
XM_011523830.1:c.1387G>C	XP_011522132.1:p.Gly463Arg
XR_934021.1:n.1494G>C
XR_934022.1:n.1494G>C
XR_934023.1:n.1494G>C
XM_006721516.3:c.1387G>C	XP_006721579.2:p.Gly463Arg
XM_011523829.2:c.1387G>C	XP_011522131.1:p.Gly463Arg
XM_011523830.2:c.1387G>C	XP_011522132.1:p.Gly463Arg
XM_024450741.1:c.1387G>C	XP_024306509.1:p.Gly463Arg
XR_934021.2:n.1446G>C
XR_934022.2:n.1446G>C
XR_934023.2:n.1446G>C
NM_000018.4:c.1387G>C MANE Select	NP_000009.1:p.Gly463Arg
NM_001033859.3:c.1321G>C	NP_001029031.1:p.Gly441Arg
NM_001270447.2:c.1456G>C	NP_001257376.1:p.Gly486Arg
NM_001270448.2:c.1159G>C	NP_001257377.1:p.Gly387Arg