Canonical Allele Identifier: CA1339333275
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059002357

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873399dup , CM000664.2:g.240873399dup GRCh38
NC_000002.11:g.241812816dup , CM000664.1:g.241812816dup GRCh37
NC_000002.10:g.241461489dup NCBI36
NG_008005.1:g.9655dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+350dup MANE Select ENSP00000302620.3:n.595+350dup
ENST00000307503.3:c.595+350dup ENSP00000302620.3:n.595+350dup
ENST00000472436.1:n.965dup
ENST00000476698.1:n.332+350dup
NM_000030.2:c.595+350dup NP_000021.1:n.595+350dup
NM_000030.3:c.595+350dup MANE Select NP_000021.1:n.595+350dup