Canonical Allele Identifier: CA15266874

Gene: GSK3B

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119839004A>T , CM000665.2:g.119839004A>T	GRCh38
NC_000003.11:g.119557851A>T , CM000665.1:g.119557851A>T	GRCh37
NC_000003.10:g.121040541A>T	NCBI36
NG_012922.1:g.260414T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.1195+4251T>A MANE Select	ENSP00000264235.9:n.1195+4251T>A
ENST00000316626.6:c.1234+4251T>A	ENSP00000324806.5:n.1234+4251T>A
ENST00000650344.2:c.1097-12149T>A	ENSP00000497956.2:n.1097-12149T>A
ENST00000676566.1:n.1021+4251T>A
ENST00000676910.1:c.195+4251T>A	ENSP00000504338.1:n.195+4251T>A
ENST00000677502.1:n.978+4251T>A
ENST00000677959.1:n.100-727T>A
ENST00000678013.1:c.197+4251T>A
ENST00000678159.1:c.165+1793T>A
ENST00000678439.1:c.1195+4251T>A	ENSP00000503868.1:n.1195+4251T>A
ENST00000679068.1:c.238+1793T>A
ENST00000679201.1:c.97-12149T>A	ENSP00000502998.1:n.97-12149T>A
ENST00000679206.1:c.132-12149T>A	ENSP00000502943.1:n.132-12149T>A
ENST00000264235.12:c.1195+4251T>A	ENSP00000264235.8:n.1195+4251T>A
ENST00000316626.5:c.1234+4251T>A	ENSP00000324806.5:n.1234+4251T>A
ENST00000473886.1:n.284-12149T>A
ENST00000474830.1:n.355+4251T>A
NM_001146156.1:c.1195+4251T>A	NP_001139628.1:n.1195+4251T>A
NM_002093.3:c.1234+4251T>A	NP_002084.2:n.1234+4251T>A
XM_006713610.1:c.1136-12149T>A	XP_006713673.1:n.1136-12149T>A
XM_006713611.1:c.1097-12149T>A	XP_006713674.1:n.1097-12149T>A
NM_001354596.1:c.1097-12149T>A	NP_001341525.1:n.1097-12149T>A
XM_006713610.3:c.1136-12149T>A	XP_006713673.1:n.1136-12149T>A
NM_001146156.2:c.1195+4251T>A MANE Select	NP_001139628.1:n.1195+4251T>A
NM_001354596.2:c.1097-12149T>A	NP_001341525.1:n.1097-12149T>A
NM_002093.4:c.1234+4251T>A	NP_002084.2:n.1234+4251T>A