Canonical Allele Identifier: CA359403861

Gene: AGXT2

Linked Data

• MyVariant Identifiers: chr5:g.34998883A>C (hg19) ; chr5:g.34998778A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998778A>C , CM000667.2:g.34998778A>C	GRCh38
NC_000005.9:g.34998883A>C , CM000667.1:g.34998883A>C	GRCh37
NC_000005.8:g.35034640A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000231420.11:c.1486T>G MANE Select	ENSP00000231420.6:p.Phe496Val
ENST00000231420.10:c.1486T>G	ENSP00000231420.6:p.Phe496Val
ENST00000510428.1:c.1261T>G	ENSP00000422799.1:p.Phe421Val
ENST00000512135.5:n.1156T>G
ENST00000618015.4:c.1261T>G	ENSP00000479154.1:p.Phe421Val
NM_001306173.1:c.1261T>G	NP_001293102.1:p.Phe421Val
NM_031900.3:c.1486T>G	NP_114106.1:p.Phe496Val
XM_005248337.2:c.1483T>G	XP_005248394.1:p.Phe495Val
XM_005248338.2:c.1291T>G	XP_005248395.1:p.Phe431Val
XM_011514077.1:c.1438-376T>G	XP_011512379.1:n.1438-376T>G
XM_005248337.3:c.1483T>G	XP_005248394.1:p.Phe495Val
XM_005248338.3:c.1291T>G	XP_005248395.1:p.Phe431Val
XM_017009748.2:c.1261T>G	XP_016865237.1:p.Phe421Val
NM_031900.4:c.1486T>G MANE Select	NP_114106.1:p.Phe496Val
NM_001306173.2:c.1261T>G	NP_001293102.1:p.Phe421Val