Canonical Allele Identifier: CA1339331098
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869487C= , CM000664.2:g.240869487C= GRCh38
NC_000002.11:g.241808904C= , CM000664.1:g.241808904C= GRCh37
NC_000002.10:g.241457577C= NCBI36
NG_008005.1:g.5743C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.358+125C= MANE Select ENSP00000302620.3:n.358+125C=
ENST00000307503.3:c.358+125C= ENSP00000302620.3:n.358+125C=
ENST00000472436.1:n.378+125C=
NM_000030.2:c.358+125C= NP_000021.1:n.358+125C=
XR_924060.1:n.405+746G=
NM_000030.3:c.358+125C= MANE Select NP_000021.1:n.358+125C=