Canonical Allele Identifier: CA443882172

Gene: AGXT2

Linked Data

• MyVariant Identifiers: chr5:g.34998926A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998821A>G , CM000667.2:g.34998821A>G	GRCh38
NC_000005.9:g.34998926A>G , CM000667.1:g.34998926A>G	GRCh37
NC_000005.8:g.35034683A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1443T>C MANE Select	ENSP00000231420.6:p.Phe481=
ENST00000231420.10:c.1443T>C	ENSP00000231420.6:p.Phe481=
ENST00000510428.1:c.1218T>C	ENSP00000422799.1:p.Phe406=
ENST00000512135.5:n.1113T>C
ENST00000618015.4:c.1218T>C	ENSP00000479154.1:p.Phe406=
NM_001306173.1:c.1218T>C	NP_001293102.1:p.Phe406=
NM_031900.3:c.1443T>C	NP_114106.1:p.Phe481=
XM_005248337.2:c.1440T>C	XP_005248394.1:p.Phe480=
XM_005248338.2:c.1248T>C	XP_005248395.1:p.Phe416=
XM_011514077.1:c.1438-419T>C	XP_011512379.1:n.1438-419T>C
XM_005248337.3:c.1440T>C	XP_005248394.1:p.Phe480=
XM_005248338.3:c.1248T>C	XP_005248395.1:p.Phe416=
XM_017009748.2:c.1218T>C	XP_016865237.1:p.Phe406=
NM_031900.4:c.1443T>C MANE Select	NP_114106.1:p.Phe481=
NM_001306173.2:c.1218T>C	NP_001293102.1:p.Phe406=