Canonical Allele Identifier: CA351319609
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878101A>C , CM000664.2:g.240878101A>C GRCh38
NC_000002.11:g.241817518A>C , CM000664.1:g.241817518A>C GRCh37
NC_000002.10:g.241466191A>C NCBI36
NG_008005.1:g.14357A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1022A>C MANE Select ENSP00000302620.3:p.Asp341Ala
ENST00000307503.3:c.1022A>C ENSP00000302620.3:p.Asp341Ala
ENST00000470255.1:n.800A>C
NM_000030.2:c.1022A>C NP_000021.1:p.Asp341Ala
NM_000030.3:c.1022A>C MANE Select NP_000021.1:p.Asp341Ala