Canonical Allele Identifier: CA1339331015
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869349C= , CM000664.2:g.240869349C= GRCh38
NC_000002.11:g.241808766C= , CM000664.1:g.241808766C= GRCh37
NC_000002.10:g.241457439C= NCBI36
NG_008005.1:g.5605C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.345C= MANE Select ENSP00000302620.3:p.Ile115=
ENST00000307503.3:c.345C= ENSP00000302620.3:p.Ile115=
ENST00000472436.1:n.365C=
NM_000030.2:c.345C= NP_000021.1:p.Ile115=
XR_924060.1:n.405+884G=
NM_000030.3:c.345C= MANE Select NP_000021.1:p.Ile115=
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