Canonical Allele Identifier: CA359403688

Gene: AGXT2

Linked Data

• MyVariant Identifiers: chr5:g.34998858G>A (hg19) ; chr5:g.34998753G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998753G>A , CM000667.2:g.34998753G>A	GRCh38
NC_000005.9:g.34998858G>A , CM000667.1:g.34998858G>A	GRCh37
NC_000005.8:g.35034615G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1511C>T MANE Select	ENSP00000231420.6:p.Ala504Val
ENST00000231420.10:c.1511C>T	ENSP00000231420.6:p.Ala504Val
ENST00000510428.1:c.1286C>T	ENSP00000422799.1:p.Ala429Val
ENST00000512135.5:n.1181C>T
ENST00000618015.4:c.1286C>T	ENSP00000479154.1:p.Ala429Val
NM_001306173.1:c.1286C>T	NP_001293102.1:p.Ala429Val
NM_031900.3:c.1511C>T	NP_114106.1:p.Ala504Val
XM_005248337.2:c.1508C>T	XP_005248394.1:p.Ala503Val
XM_005248338.2:c.1316C>T	XP_005248395.1:p.Ala439Val
XM_011514077.1:c.1438-351C>T	XP_011512379.1:n.1438-351C>T
XM_005248337.3:c.1508C>T	XP_005248394.1:p.Ala503Val
XM_005248338.3:c.1316C>T	XP_005248395.1:p.Ala439Val
XM_017009748.2:c.1286C>T	XP_016865237.1:p.Ala429Val
NM_031900.4:c.1511C>T MANE Select	NP_114106.1:p.Ala504Val
NM_001306173.2:c.1286C>T	NP_001293102.1:p.Ala429Val