Canonical Allele Identifier: CA1052775353

Gene: GSK3B

Linked Data

• dbSNP Id: rs2056507576
• gnomAD v3: 3-119891955-GTTAGAAAT-G
• gnomAD v4: 3-119891955-GTTAGAAAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119891959_119891966del , CM000665.2:g.119891959_119891966del	GRCh38
NC_000003.11:g.119610806_119610813del , CM000665.1:g.119610806_119610813del	GRCh37
NC_000003.10:g.121093496_121093503del	NCBI36
NG_012922.1:g.207455_207462del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264235.13:c.813+13792_813+13799del MANE Select	ENSP00000264235.9:n.813+13792_813+13799del
ENST00000316626.6:c.813+13792_813+13799del	ENSP00000324806.5:n.813+13792_813+13799del
ENST00000650344.2:c.813+13792_813+13799del	ENSP00000497956.2:n.813+13792_813+13799del
ENST00000676566.1:n.639+13792_639+13799del
ENST00000676887.1:c.132-15455_132-15448del	ENSP00000502977.1:n.132-15455_132-15448del
ENST00000676948.1:c.154+8595_154+8602del
ENST00000677046.1:c.98+13792_98+13799del
ENST00000677069.1:c.99-11465_99-11458del
ENST00000677362.1:c.107+20741_107+20748del
ENST00000677483.1:c.99-9129_99-9122del
ENST00000677502.1:n.596+13792_596+13799del
ENST00000677648.1:c.99-11453_99-11446del
ENST00000677716.1:c.131+24081_131+24088del	ENSP00000503671.1:n.131+24081_131+24088del
ENST00000677788.1:n.1283-11465_1283-11458del
ENST00000677995.1:c.326+13792_326+13799del	ENSP00000504203.1:n.326+13792_326+13799del
ENST00000678013.1:c.98+13792_98+13799del
ENST00000678181.1:c.85-28358_85-28351del	ENSP00000504266.1:n.85-28358_85-28351del
ENST00000678377.1:c.229+13792_229+13799del	ENSP00000503164.1:n.229+13792_229+13799del
ENST00000678439.1:c.813+13792_813+13799del	ENSP00000503868.1:n.813+13792_813+13799del
ENST00000678509.1:c.99-9129_99-9122del
ENST00000678561.1:c.486+13792_486+13799del	ENSP00000503494.1:n.486+13792_486+13799del
ENST00000678754.1:n.99-7581_99-7574del
ENST00000678787.1:c.195-15455_195-15448del
ENST00000679066.1:c.85-15455_85-15448del	ENSP00000503626.1:n.85-15455_85-15448del
ENST00000679188.1:c.112-15455_112-15448del	ENSP00000504252.1:n.112-15455_112-15448del
ENST00000679194.1:c.108-15455_108-15448del
ENST00000679206.1:c.131+24081_131+24088del	ENSP00000502943.1:n.131+24081_131+24088del
ENST00000264235.12:c.813+13792_813+13799del	ENSP00000264235.8:n.813+13792_813+13799del
ENST00000316626.5:c.813+13792_813+13799del	ENSP00000324806.5:n.813+13792_813+13799del
NM_001146156.1:c.813+13792_813+13799del	NP_001139628.1:n.813+13792_813+13799del
NM_002093.3:c.813+13792_813+13799del	NP_002084.2:n.813+13792_813+13799del
XM_006713610.1:c.813+13792_813+13799del	XP_006713673.1:n.813+13792_813+13799del
XM_006713611.1:c.813+13792_813+13799del	XP_006713674.1:n.813+13792_813+13799del
NM_001354596.1:c.813+13792_813+13799del	NP_001341525.1:n.813+13792_813+13799del
XM_006713610.3:c.813+13792_813+13799del	XP_006713673.1:n.813+13792_813+13799del
NM_001146156.2:c.813+13792_813+13799del MANE Select	NP_001139628.1:n.813+13792_813+13799del
NM_001354596.2:c.813+13792_813+13799del	NP_001341525.1:n.813+13792_813+13799del
NM_002093.4:c.813+13792_813+13799del	NP_002084.2:n.813+13792_813+13799del