Canonical Allele Identifier: CA2664012692
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878844_240878860dup , CM000664.2:g.240878844_240878860dup GRCh38
NC_000002.11:g.241818261_241818277dup , CM000664.1:g.241818261_241818277dup GRCh37
NC_000002.10:g.241466934_241466950dup NCBI36
NG_008005.1:g.15100_15116dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*23_*39dup MANE Select ENSP00000302620.3:n.*23_*39dup
ENST00000307503.3:c.*23_*39dup ENSP00000302620.3:n.*23_*39dup
ENST00000470255.1:n.980_996dup
NM_000030.2:c.*23_*39dup NP_000021.1:n.*23_*39dup
NM_000030.3:c.*23_*39dup MANE Select NP_000021.1:n.*23_*39dup