Canonical Allele Identifier: CA1339330783

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240868965C= , CM000664.2:g.240868965C=	GRCh38
NC_000002.11:g.241808382C= , CM000664.1:g.241808382C=	GRCh37
NC_000002.10:g.241457055C=	NCBI36
NG_008005.1:g.5221C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.100C= MANE Select	ENSP00000302620.3:p.Pro34=
ENST00000307503.3:c.100C=	ENSP00000302620.3:p.Pro34=
ENST00000472436.1:n.120C=
NM_000030.2:c.100C=	NP_000021.1:p.Pro34=
XR_924060.1:n.405+1268G=
NM_000030.3:c.100C= MANE Select	NP_000021.1:p.Pro34=