Canonical Allele Identifier: CA1339333155
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873156_240873159delinsGCCC , CM000664.2:g.240873156_240873159delinsGCCC GRCh38
NC_000002.11:g.241812573_241812576delinsGCCC , CM000664.1:g.241812573_241812576delinsGCCC GRCh37
NC_000002.10:g.241461246_241461249delinsGCCC NCBI36
NG_008005.1:g.9412_9415delinsGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+107_595+110delinsGCCC MANE Select ENSP00000302620.3:n.595+107_595+110delinsGCCC
ENST00000307503.3:c.595+107_595+110delinsGCCC ENSP00000302620.3:n.595+107_595+110delinsGCCC
ENST00000472436.1:n.722_725delinsGCCC
ENST00000476698.1:n.332+107_332+110delinsGCCC
NM_000030.2:c.595+107_595+110delinsGCCC NP_000021.1:n.595+107_595+110delinsGCCC
NM_000030.3:c.595+107_595+110delinsGCCC MANE Select NP_000021.1:n.595+107_595+110delinsGCCC