Canonical Allele Identifier: CA1339334297

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875351T= , CM000664.2:g.240875351T=	GRCh38
NC_000002.11:g.241814768T= , CM000664.1:g.241814768T=	GRCh37
NC_000002.10:g.241463441T=	NCBI36
NG_008005.1:g.11607T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.776+147T= MANE Select	ENSP00000302620.3:n.776+147T=
ENST00000307503.3:c.776+147T=	ENSP00000302620.3:n.776+147T=
ENST00000476698.1:n.428+147T=
NM_000030.2:c.776+147T=	NP_000021.1:n.776+147T=
NM_000030.3:c.776+147T= MANE Select	NP_000021.1:n.776+147T=