Canonical Allele Identifier: CA441363162

Gene: AFG2A

Linked Data

• MyVariant Identifiers: chr4:g.123868457C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122947302C>A , CM000666.2:g.122947302C>A	GRCh38
NC_000004.11:g.123868457C>A , CM000666.1:g.123868457C>A	GRCh37
NC_000004.10:g.124087907C>A	NCBI36
NG_051570.1:g.29233C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274008.5:c.1528C>A MANE Select	ENSP00000274008.3:p.Arg510=
ENST00000674886.1:n.1590C>A
ENST00000675612.1:c.1525C>A	ENSP00000502453.1:p.Arg509=
ENST00000274008.4:c.1528C>A	ENSP00000274008.3:p.Arg510=
ENST00000422835.2:n.1570C>A
NM_145207.2:c.1528C>A	NP_660208.2:p.Arg510=
XM_005262783.3:c.1525C>A	XP_005262840.1:p.Arg509=
XM_011531678.1:c.1525C>A	XP_011529980.1:p.Arg509=
XM_011531679.1:c.1528C>A	XP_011529981.1:p.Arg510=
NM_001317799.1:c.1525C>A	NP_001304728.1:p.Arg509=
NM_001345856.1:c.1525C>A	NP_001332785.1:p.Arg509=
XM_011531678.2:c.1525C>A	XP_011529980.1:p.Arg509=
XM_011531679.3:c.1528C>A	XP_011529981.1:p.Arg510=
XM_017007825.1:c.1528C>A	XP_016863314.1:p.Arg510=
XM_017007826.1:c.1528C>A	XP_016863315.1:p.Arg510=
XM_017007827.2:c.1528C>A	XP_016863316.1:p.Arg510=
XM_017007828.1:c.1306C>A	XP_016863317.1:p.Arg436=
XM_017007829.1:c.1072C>A	XP_016863318.1:p.Arg358=
XM_017007830.1:c.1528C>A	XP_016863319.1:p.Arg510=
XR_001741151.1:n.1598C>A
NM_145207.3:c.1528C>A MANE Select	NP_660208.2:p.Arg510=
NM_001317799.2:c.1525C>A	NP_001304728.1:p.Arg509=
NM_001345856.2:c.1525C>A	NP_001332785.1:p.Arg509=