Canonical Allele Identifier: CA1339333028
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240872911T= , CM000664.2:g.240872911T= GRCh38
NC_000002.11:g.241812328T= , CM000664.1:g.241812328T= GRCh37
NC_000002.10:g.241461001T= NCBI36
NG_008005.1:g.9167T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.525-68T= MANE Select ENSP00000302620.3:n.525-68T=
ENST00000307503.3:c.525-68T= ENSP00000302620.3:n.525-68T=
ENST00000472436.1:n.545-68T=
ENST00000476698.1:n.262-68T=
NM_000030.2:c.525-68T= NP_000021.1:n.525-68T=
NM_000030.3:c.525-68T= MANE Select NP_000021.1:n.525-68T=