Canonical Allele Identifier: CA1396824342

Gene: GSK3B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120027786G= , CM000665.2:g.120027786G=	GRCh38
NC_000003.11:g.119746633G= , CM000665.1:g.119746633G=	GRCh37
NC_000003.10:g.121229323G=	NCBI36
NG_012922.1:g.71632C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.89-25547C= MANE Select	ENSP00000264235.9:n.89-25547C=
ENST00000316626.6:c.89-25547C=	ENSP00000324806.5:n.89-25547C=
ENST00000650344.2:c.89-25547C=	ENSP00000497956.2:n.89-25547C=
ENST00000677034.1:c.89-6160C=	ENSP00000504055.1:n.89-6160C=
ENST00000677128.1:c.93-25550C=	ENSP00000503177.1:n.93-25550C=
ENST00000677169.1:c.88+65561C=	ENSP00000503107.1:n.88+65561C=
ENST00000677530.1:n.546-25547C=
ENST00000677788.1:n.558-25547C=
ENST00000678245.1:n.546-25547C=
ENST00000678439.1:c.89-25547C=	ENSP00000503868.1:n.89-25547C=
ENST00000679131.1:n.31-25547C=
ENST00000264235.12:c.89-25547C=	ENSP00000264235.8:n.89-25547C=
ENST00000316626.5:c.89-25547C=	ENSP00000324806.5:n.89-25547C=
NM_001146156.1:c.89-25547C=	NP_001139628.1:n.89-25547C=
NM_002093.3:c.89-25547C=	NP_002084.2:n.89-25547C=
XM_006713610.1:c.89-25547C=	XP_006713673.1:n.89-25547C=
XM_006713611.1:c.89-25547C=	XP_006713674.1:n.89-25547C=
NM_001354596.1:c.89-25547C=	NP_001341525.1:n.89-25547C=
XM_006713610.3:c.89-25547C=	XP_006713673.1:n.89-25547C=
XR_002959518.1:n.2478-25547C=
NM_001146156.2:c.89-25547C= MANE Select	NP_001139628.1:n.89-25547C=
NM_001354596.2:c.89-25547C=	NP_001341525.1:n.89-25547C=
NM_002093.4:c.89-25547C=	NP_002084.2:n.89-25547C=