Canonical Allele Identifier: CA1339335849

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240878203C= , CM000664.2:g.240878203C=	GRCh38
NC_000002.11:g.241817620C= , CM000664.1:g.241817620C=	GRCh37
NC_000002.10:g.241466293C=	NCBI36
NG_008005.1:g.14459C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.1071+53C= MANE Select	ENSP00000302620.3:n.1071+53C=
ENST00000307503.3:c.1071+53C=	ENSP00000302620.3:n.1071+53C=
ENST00000470255.1:n.849+53C=
NM_000030.2:c.1071+53C=	NP_000021.1:n.1071+53C=
NM_000030.3:c.1071+53C= MANE Select	NP_000021.1:n.1071+53C=