Canonical Allele Identifier: CA1339330733
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868868G= , CM000664.2:g.240868868G= GRCh38
NC_000002.11:g.241808285G= , CM000664.1:g.241808285G= GRCh37
NC_000002.10:g.241456958G= NCBI36
NG_008005.1:g.5124G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.3G= MANE Select ENSP00000302620.3:p.Met1=
ENST00000307503.3:c.3G= ENSP00000302620.3:p.Met1=
ENST00000472436.1:n.23G=
NM_000030.2:c.3G= NP_000021.1:p.Met1=
XR_924060.1:n.405+1365C=
NM_000030.3:c.3G= MANE Select NP_000021.1:p.Met1=