Canonical Allele Identifier: CA2667150592
Gene: GSK3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120094334_120094435del , CM000665.2:g.120094334_120094435del GRCh38
NC_000003.11:g.119813181_119813282del , CM000665.1:g.119813181_119813282del GRCh37
NC_000003.10:g.121295871_121295972del NCBI36
NG_012922.1:g.4983_5084del

Transcript Alleles

HGVS Amino-acid change
ENST00000264235.13:c.-1001_-900del MANE Select ENSP00000264235.9:n.-1001_-900del
ENST00000677034.1:c.-1001_-900del ENSP00000504055.1:n.-1001_-900del
ENST00000677338.1:c.-160+531_-160+632del ENSP00000503497.1:n.-160+531_-160+632del
ENST00000677903.1:c.-160+108_-160+209del ENSP00000503112.1:n.-160+108_-160+209del
XR_002959518.1:n.1389_1490del
NM_001146156.2:c.-1001_-900del MANE Select NP_001139628.1:n.-1001_-900del
NM_001354596.2:c.-1001_-900del NP_001341525.1:n.-1001_-900del
NM_002093.4:c.-1001_-900del NP_002084.2:n.-1001_-900del