Canonical Allele Identifier: CA1339333266

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240873384T= , CM000664.2:g.240873384T=	GRCh38
NC_000002.11:g.241812801T= , CM000664.1:g.241812801T=	GRCh37
NC_000002.10:g.241461474T=	NCBI36
NG_008005.1:g.9640T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.595+335T= MANE Select	ENSP00000302620.3:n.595+335T=
ENST00000307503.3:c.595+335T=	ENSP00000302620.3:n.595+335T=
ENST00000472436.1:n.950T=
ENST00000476698.1:n.332+335T=
NM_000030.2:c.595+335T=	NP_000021.1:n.595+335T=
NM_000030.3:c.595+335T= MANE Select	NP_000021.1:n.595+335T=