Canonical Allele Identifier: CA1339336276
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879039_240879040delinsAG , CM000664.2:g.240879039_240879040delinsAG GRCh38
NC_000002.11:g.241818456_241818457delinsAG , CM000664.1:g.241818456_241818457delinsAG GRCh37
NC_000002.10:g.241467129_241467130delinsAG NCBI36
NG_008005.1:g.15295_15296delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*218_*219delinsAG MANE Select ENSP00000302620.3:n.*218_*219delinsAG
ENST00000307503.3:c.*218_*219delinsAG ENSP00000302620.3:n.*218_*219delinsAG
ENST00000470255.1:n.1175_1176delinsAG
NM_000030.2:c.*218_*219delinsAG NP_000021.1:n.*218_*219delinsAG
NM_000030.3:c.*218_*219delinsAG MANE Select NP_000021.1:n.*218_*219delinsAG