Canonical Allele Identifier: CA1339336214
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878902C= , CM000664.2:g.240878902C= GRCh38
NC_000002.11:g.241818319C= , CM000664.1:g.241818319C= GRCh37
NC_000002.10:g.241466992C= NCBI36
NG_008005.1:g.15158C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*81C= MANE Select ENSP00000302620.3:n.*81C=
ENST00000307503.3:c.*81C= ENSP00000302620.3:n.*81C=
ENST00000470255.1:n.1038C=
NM_000030.2:c.*81C= NP_000021.1:n.*81C=
NM_000030.3:c.*81C= MANE Select NP_000021.1:n.*81C=
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