Canonical Allele Identifier: CA1339330813

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240869010A= , CM000664.2:g.240869010A=	GRCh38
NC_000002.11:g.241808427A= , CM000664.1:g.241808427A=	GRCh37
NC_000002.10:g.241457100A=	NCBI36
NG_008005.1:g.5266A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.145A= MANE Select	ENSP00000302620.3:p.Met49=
ENST00000307503.3:c.145A=	ENSP00000302620.3:p.Met49=
ENST00000472436.1:n.165A=
NM_000030.2:c.145A=	NP_000021.1:p.Met49=
XR_924060.1:n.405+1223T=
NM_000030.3:c.145A= MANE Select	NP_000021.1:p.Met49=