Canonical Allele Identifier: CA441363275

Gene: AFG2A

Linked Data

• MyVariant Identifiers: chr4:g.123868516G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122947361G>C , CM000666.2:g.122947361G>C	GRCh38
NC_000004.11:g.123868516G>C , CM000666.1:g.123868516G>C	GRCh37
NC_000004.10:g.124087966G>C	NCBI36
NG_051570.1:g.29292G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000274008.5:c.1587G>C MANE Select	ENSP00000274008.3:p.Arg529=
ENST00000674886.1:n.1649G>C
ENST00000675612.1:c.1584G>C	ENSP00000502453.1:p.Arg528=
ENST00000274008.4:c.1587G>C	ENSP00000274008.3:p.Arg529=
ENST00000422835.2:n.1629G>C
NM_145207.2:c.1587G>C	NP_660208.2:p.Arg529=
XM_005262783.3:c.1584G>C	XP_005262840.1:p.Arg528=
XM_011531678.1:c.1584G>C	XP_011529980.1:p.Arg528=
XM_011531679.1:c.1587G>C	XP_011529981.1:p.Arg529=
NM_001317799.1:c.1584G>C	NP_001304728.1:p.Arg528=
NM_001345856.1:c.1584G>C	NP_001332785.1:p.Arg528=
XM_011531678.2:c.1584G>C	XP_011529980.1:p.Arg528=
XM_011531679.3:c.1587G>C	XP_011529981.1:p.Arg529=
XM_017007825.1:c.1587G>C	XP_016863314.1:p.Arg529=
XM_017007826.1:c.1587G>C	XP_016863315.1:p.Arg529=
XM_017007827.2:c.1587G>C	XP_016863316.1:p.Arg529=
XM_017007828.1:c.1365G>C	XP_016863317.1:p.Arg455=
XM_017007829.1:c.1131G>C	XP_016863318.1:p.Arg377=
XM_017007830.1:c.1587G>C	XP_016863319.1:p.Arg529=
XR_001741151.1:n.1657G>C
NM_145207.3:c.1587G>C MANE Select	NP_660208.2:p.Arg529=
NM_001317799.2:c.1584G>C	NP_001304728.1:p.Arg528=
NM_001345856.2:c.1584G>C	NP_001332785.1:p.Arg528=