Canonical Allele Identifier: CA1339335726
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877993C= , CM000664.2:g.240877993C= GRCh38
NC_000002.11:g.241817410C= , CM000664.1:g.241817410C= GRCh37
NC_000002.10:g.241466083C= NCBI36
NG_008005.1:g.14249C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-29C= MANE Select ENSP00000302620.3:n.943-29C=
ENST00000307503.3:c.943-29C= ENSP00000302620.3:n.943-29C=
ENST00000470255.1:n.721-29C=
NM_000030.2:c.943-29C= NP_000021.1:n.943-29C=
NM_000030.3:c.943-29C= MANE Select NP_000021.1:n.943-29C=