Canonical Allele Identifier: CA359403470

Gene: AGXT2

Linked Data

• gnomAD v4: 5-34998726-G-T
• MyVariant Identifiers: chr5:g.34998831G>T (hg19) ; chr5:g.34998726G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998726G>T , CM000667.2:g.34998726G>T	GRCh38
NC_000005.9:g.34998831G>T , CM000667.1:g.34998831G>T	GRCh37
NC_000005.8:g.35034588G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1538C>A MANE Select	ENSP00000231420.6:p.Ala513Asp
ENST00000231420.10:c.1538C>A	ENSP00000231420.6:p.Ala513Asp
ENST00000510428.1:c.1313C>A	ENSP00000422799.1:p.Ala438Asp
ENST00000512135.5:n.1208C>A
ENST00000618015.4:c.1313C>A	ENSP00000479154.1:p.Ala438Asp
NM_001306173.1:c.1313C>A	NP_001293102.1:p.Ala438Asp
NM_031900.3:c.1538C>A	NP_114106.1:p.Ala513Asp
XM_005248337.2:c.1535C>A	XP_005248394.1:p.Ala512Asp
XM_005248338.2:c.1343C>A	XP_005248395.1:p.Ala448Asp
XM_011514077.1:c.1438-324C>A	XP_011512379.1:n.1438-324C>A
XM_005248337.3:c.1535C>A	XP_005248394.1:p.Ala512Asp
XM_005248338.3:c.1343C>A	XP_005248395.1:p.Ala448Asp
XM_017009748.2:c.1313C>A	XP_016865237.1:p.Ala438Asp
NM_031900.4:c.1538C>A MANE Select	NP_114106.1:p.Ala513Asp
NM_001306173.2:c.1313C>A	NP_001293102.1:p.Ala438Asp