Canonical Allele Identifier: CA1339335521
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877574C= , CM000664.2:g.240877574C= GRCh38
NC_000002.11:g.241816991C= , CM000664.1:g.241816991C= GRCh37
NC_000002.10:g.241465664C= NCBI36
NG_008005.1:g.13830C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.884C= MANE Select ENSP00000302620.3:p.Ala295=
ENST00000307503.3:c.884C= ENSP00000302620.3:p.Ala295=
ENST00000470255.1:n.662C=
NM_000030.2:c.884C= NP_000021.1:p.Ala295=
NM_000030.3:c.884C= MANE Select NP_000021.1:p.Ala295=
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