Canonical Allele Identifier: CA351319884
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878802G>A , CM000664.2:g.240878802G>A GRCh38
NC_000002.11:g.241818219G>A , CM000664.1:g.241818219G>A GRCh37
NC_000002.10:g.241466892G>A NCBI36
NG_008005.1:g.15058G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1160G>A MANE Select ENSP00000302620.3:p.Cys387Tyr
ENST00000307503.3:c.1160G>A ENSP00000302620.3:p.Cys387Tyr
ENST00000470255.1:n.938G>A
NM_000030.2:c.1160G>A NP_000021.1:p.Cys387Tyr
NM_000030.3:c.1160G>A MANE Select NP_000021.1:p.Cys387Tyr