Canonical Allele Identifier: CA359403889

Gene: AGXT2

Linked Data

• MyVariant Identifiers: chr5:g.34998886C>A (hg19) ; chr5:g.34998781C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998781C>A , CM000667.2:g.34998781C>A	GRCh38
NC_000005.9:g.34998886C>A , CM000667.1:g.34998886C>A	GRCh37
NC_000005.8:g.35034643C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000231420.11:c.1483G>T MANE Select	ENSP00000231420.6:p.Asp495Tyr
ENST00000231420.10:c.1483G>T	ENSP00000231420.6:p.Asp495Tyr
ENST00000510428.1:c.1258G>T	ENSP00000422799.1:p.Asp420Tyr
ENST00000512135.5:n.1153G>T
ENST00000618015.4:c.1258G>T	ENSP00000479154.1:p.Asp420Tyr
NM_001306173.1:c.1258G>T	NP_001293102.1:p.Asp420Tyr
NM_031900.3:c.1483G>T	NP_114106.1:p.Asp495Tyr
XM_005248337.2:c.1480G>T	XP_005248394.1:p.Asp494Tyr
XM_005248338.2:c.1288G>T	XP_005248395.1:p.Asp430Tyr
XM_011514077.1:c.1438-379G>T	XP_011512379.1:n.1438-379G>T
XM_005248337.3:c.1480G>T	XP_005248394.1:p.Asp494Tyr
XM_005248338.3:c.1288G>T	XP_005248395.1:p.Asp430Tyr
XM_017009748.2:c.1258G>T	XP_016865237.1:p.Asp420Tyr
NM_031900.4:c.1483G>T MANE Select	NP_114106.1:p.Asp495Tyr
NM_001306173.2:c.1258G>T	NP_001293102.1:p.Asp420Tyr