Canonical Allele Identifier: CA1396770589

Gene: GSK3B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119912967A= , CM000665.2:g.119912967A=	GRCh38
NC_000003.11:g.119631814A= , CM000665.1:g.119631814A=	GRCh37
NC_000003.10:g.121114504A=	NCBI36
NG_012922.1:g.186451T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.609-157T= MANE Select	ENSP00000264235.9:n.609-157T=
ENST00000316626.6:c.609-157T=	ENSP00000324806.5:n.609-157T=
ENST00000650344.2:c.609-157T=	ENSP00000497956.2:n.609-157T=
ENST00000676566.1:n.435-157T=
ENST00000676733.1:c.136-157T=	ENSP00000504716.1:n.136-157T=
ENST00000676887.1:c.131+3077T=	ENSP00000502977.1:n.131+3077T=
ENST00000677400.1:c.132-217T=	ENSP00000504538.1:n.132-217T=
ENST00000677502.1:n.392-157T=
ENST00000677716.1:c.131+3077T=	ENSP00000503671.1:n.131+3077T=
ENST00000677788.1:n.1078-157T=
ENST00000677995.1:c.132-167T=	ENSP00000504203.1:n.132-167T=
ENST00000678181.1:c.84+34301T=	ENSP00000504266.1:n.84+34301T=
ENST00000678245.1:n.1066-157T=
ENST00000678377.1:c.131+3077T=	ENSP00000503164.1:n.131+3077T=
ENST00000678439.1:c.609-157T=	ENSP00000503868.1:n.609-157T=
ENST00000678561.1:c.282-157T=	ENSP00000503494.1:n.282-157T=
ENST00000678787.1:c.195-36459T=
ENST00000679066.1:c.84+34301T=	ENSP00000503626.1:n.84+34301T=
ENST00000679188.1:c.111+10406T=	ENSP00000504252.1:n.111+10406T=
ENST00000679206.1:c.131+3077T=	ENSP00000502943.1:n.131+3077T=
ENST00000264235.12:c.609-157T=	ENSP00000264235.8:n.609-157T=
ENST00000316626.5:c.609-157T=	ENSP00000324806.5:n.609-157T=
NM_001146156.1:c.609-157T=	NP_001139628.1:n.609-157T=
NM_002093.3:c.609-157T=	NP_002084.2:n.609-157T=
XM_006713610.1:c.609-157T=	XP_006713673.1:n.609-157T=
XM_006713611.1:c.609-157T=	XP_006713674.1:n.609-157T=
NM_001354596.1:c.609-157T=	NP_001341525.1:n.609-157T=
XM_006713610.3:c.609-157T=	XP_006713673.1:n.609-157T=
NM_001146156.2:c.609-157T= MANE Select	NP_001139628.1:n.609-157T=
NM_001354596.2:c.609-157T=	NP_001341525.1:n.609-157T=
NM_002093.4:c.609-157T=	NP_002084.2:n.609-157T=