Canonical Allele Identifier: CA11417374
Gene: GSK3B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119993874A>G , CM000665.2:g.119993874A>G GRCh38
NC_000003.11:g.119712721A>G , CM000665.1:g.119712721A>G GRCh37
NC_000003.10:g.121195411A>G NCBI36
NG_012922.1:g.105544T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264235.13:c.282+8172T>C MANE Select ENSP00000264235.9:n.282+8172T>C
ENST00000316626.6:c.282+8172T>C ENSP00000324806.5:n.282+8172T>C
ENST00000650344.2:c.282+8172T>C ENSP00000497956.2:n.282+8172T>C
ENST00000676775.1:c.194+8172T>C
ENST00000677128.1:c.*103+8172T>C ENSP00000503177.1:n.*103+8172T>C
ENST00000677169.1:c.89-46523T>C ENSP00000503107.1:n.89-46523T>C
ENST00000677788.1:n.751+8172T>C
ENST00000677878.1:c.194+8172T>C
ENST00000678245.1:n.739+8172T>C
ENST00000678350.1:c.194+8172T>C
ENST00000678439.1:c.282+8172T>C ENSP00000503868.1:n.282+8172T>C
ENST00000678608.1:c.366+6678T>C
ENST00000678787.1:c.194+8172T>C
ENST00000264235.12:c.282+8172T>C ENSP00000264235.8:n.282+8172T>C
ENST00000316626.5:c.282+8172T>C ENSP00000324806.5:n.282+8172T>C
NM_001146156.1:c.282+8172T>C NP_001139628.1:n.282+8172T>C
NM_002093.3:c.282+8172T>C NP_002084.2:n.282+8172T>C
XM_006713610.1:c.282+8172T>C XP_006713673.1:n.282+8172T>C
XM_006713611.1:c.282+8172T>C XP_006713674.1:n.282+8172T>C
NM_001354596.1:c.282+8172T>C NP_001341525.1:n.282+8172T>C
XM_006713610.3:c.282+8172T>C XP_006713673.1:n.282+8172T>C
NM_001146156.2:c.282+8172T>C MANE Select NP_001139628.1:n.282+8172T>C
NM_001354596.2:c.282+8172T>C NP_001341525.1:n.282+8172T>C
NM_002093.4:c.282+8172T>C NP_002084.2:n.282+8172T>C
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