Canonical Allele Identifier: CA1396762278

Gene: GSK3B

Linked Data

• dbSNP Id: rs2056507853

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119891971_119891974del , CM000665.2:g.119891971_119891974del	GRCh38
NC_000003.11:g.119610818_119610821del , CM000665.1:g.119610818_119610821del	GRCh37
NC_000003.10:g.121093508_121093511del	NCBI36
NG_012922.1:g.207446_207449del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.813+13783_813+13786del MANE Select	ENSP00000264235.9:n.813+13783_813+13786del
ENST00000316626.6:c.813+13783_813+13786del	ENSP00000324806.5:n.813+13783_813+13786del
ENST00000650344.2:c.813+13783_813+13786del	ENSP00000497956.2:n.813+13783_813+13786del
ENST00000676566.1:n.639+13783_639+13786del
ENST00000676887.1:c.132-15464_132-15461del	ENSP00000502977.1:n.132-15464_132-15461del
ENST00000676948.1:c.154+8586_154+8589del
ENST00000677046.1:c.98+13783_98+13786del
ENST00000677069.1:c.99-11474_99-11471del
ENST00000677362.1:c.107+20732_107+20735del
ENST00000677483.1:c.99-9138_99-9135del
ENST00000677502.1:n.596+13783_596+13786del
ENST00000677648.1:c.99-11462_99-11459del
ENST00000677716.1:c.131+24072_131+24075del	ENSP00000503671.1:n.131+24072_131+24075del
ENST00000677788.1:n.1283-11474_1283-11471del
ENST00000677995.1:c.326+13783_326+13786del	ENSP00000504203.1:n.326+13783_326+13786del
ENST00000678013.1:c.98+13783_98+13786del
ENST00000678181.1:c.85-28367_85-28364del	ENSP00000504266.1:n.85-28367_85-28364del
ENST00000678377.1:c.229+13783_229+13786del	ENSP00000503164.1:n.229+13783_229+13786del
ENST00000678439.1:c.813+13783_813+13786del	ENSP00000503868.1:n.813+13783_813+13786del
ENST00000678509.1:c.99-9138_99-9135del
ENST00000678561.1:c.486+13783_486+13786del	ENSP00000503494.1:n.486+13783_486+13786del
ENST00000678754.1:n.99-7590_99-7587del
ENST00000678787.1:c.195-15464_195-15461del
ENST00000679066.1:c.85-15464_85-15461del	ENSP00000503626.1:n.85-15464_85-15461del
ENST00000679188.1:c.112-15464_112-15461del	ENSP00000504252.1:n.112-15464_112-15461del
ENST00000679194.1:c.108-15464_108-15461del
ENST00000679206.1:c.131+24072_131+24075del	ENSP00000502943.1:n.131+24072_131+24075del
ENST00000264235.12:c.813+13783_813+13786del	ENSP00000264235.8:n.813+13783_813+13786del
ENST00000316626.5:c.813+13783_813+13786del	ENSP00000324806.5:n.813+13783_813+13786del
NM_001146156.1:c.813+13783_813+13786del	NP_001139628.1:n.813+13783_813+13786del
NM_002093.3:c.813+13783_813+13786del	NP_002084.2:n.813+13783_813+13786del
XM_006713610.1:c.813+13783_813+13786del	XP_006713673.1:n.813+13783_813+13786del
XM_006713611.1:c.813+13783_813+13786del	XP_006713674.1:n.813+13783_813+13786del
NM_001354596.1:c.813+13783_813+13786del	NP_001341525.1:n.813+13783_813+13786del
XM_006713610.3:c.813+13783_813+13786del	XP_006713673.1:n.813+13783_813+13786del
NM_001146156.2:c.813+13783_813+13786del MANE Select	NP_001139628.1:n.813+13783_813+13786del
NM_001354596.2:c.813+13783_813+13786del	NP_001341525.1:n.813+13783_813+13786del
NM_002093.4:c.813+13783_813+13786del	NP_002084.2:n.813+13783_813+13786del