Canonical Allele Identifier: CA1339332106

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240871406G= , CM000664.2:g.240871406G=	GRCh38
NC_000002.11:g.241810823G= , CM000664.1:g.241810823G=	GRCh37
NC_000002.10:g.241459496G=	NCBI36
NG_008005.1:g.7662G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.481G= MANE Select	ENSP00000302620.3:p.Gly161=
ENST00000307503.3:c.481G=	ENSP00000302620.3:p.Gly161=
ENST00000472436.1:n.501G=
ENST00000476698.1:n.218G=
NM_000030.2:c.481G=	NP_000021.1:p.Gly161=
NM_000030.3:c.481G= MANE Select	NP_000021.1:p.Gly161=