Canonical Allele Identifier: CA351319174
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.884C>A MANE Select ENSP00000302620.3:p.Ala295Glu
ENST00000307503.3:c.884C>A ENSP00000302620.3:p.Ala295Glu
ENST00000470255.1:n.662C>A
NM_000030.2:c.884C>A NP_000021.1:p.Ala295Glu
NM_000030.3:c.884C>A MANE Select NP_000021.1:p.Ala295Glu