Canonical Allele Identifier: CA918396565
Gene: SMARCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1586721643

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2116031_2116032insGGT , CM000671.2:g.2116031_2116032insGGT GRCh38
NC_000009.11:g.2116031_2116032insGGT , CM000671.1:g.2116031_2116032insGGT GRCh37
NC_000009.10:g.2106031_2106032insGGT NCBI36
NG_032162.1:g.105690_105691insGGT
NG_032162.2:g.140742_140743insGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3306_3307insGGT ENSP00000515861.1:p.Glu1102_His1103insGly
ENST00000704352.1:c.1174-45655_1174-45654insGGT ENSP00000515863.1:n.1174-45655_1174-45654insGGT
ENST00000704353.1:c.1174-45655_1174-45654insGGT ENSP00000515864.1:n.1174-45655_1174-45654insGGT
ENST00000704354.1:c.3650_3651insGGT
ENST00000704355.1:c.2030_2031insGGT
ENST00000349721.8:c.3666_3667insGGT MANE Select ENSP00000265773.5:p.Glu1222_His1223insGly
ENST00000357248.8:c.3666_3667insGGT ENSP00000349788.2:p.Glu1222_His1223insGly
ENST00000635739.1:n.2334_2335insGGT
ENST00000636157.1:n.1273_1274insGGT
ENST00000638139.1:n.700_701insGGT
ENST00000349721.7:c.3666_3667insGGT ENSP00000265773.5:p.Glu1222_His1223insGly
ENST00000357248.7:c.3666_3667insGGT ENSP00000349788.2:p.Glu1222_His1223insGly
ENST00000382194.6:c.3666_3667insGGT ENSP00000371629.1:p.Glu1222_His1223insGly
ENST00000382203.5:c.3666_3667insGGT ENSP00000371638.1:p.Glu1222_His1223insGly
ENST00000450198.6:c.3492_3493insGGT ENSP00000392081.2:p.Glu1164_His1165insGly
ENST00000634760.1:c.3666_3667insGGT ENSP00000489256.1:p.Glu1222_His1223insGly
ENST00000634772.1:c.62-3427_62-3426insGGT
ENST00000634925.1:n.1157_1158insGGT
NM_001289396.1:c.3666_3667insGGT NP_001276325.1:p.Glu1222_His1223insGly
NM_001289397.1:c.3492_3493insGGT NP_001276326.1:p.Glu1164_His1165insGly
NM_003070.4:c.3666_3667insGGT NP_003061.3:p.Glu1222_His1223insGly
NM_139045.3:c.3666_3667insGGT NP_620614.2:p.Glu1222_His1223insGly
NM_003070.5:c.3666_3667insGGT MANE Select NP_003061.3:p.Glu1222_His1223insGly
NM_001289397.2:c.3492_3493insGGT NP_001276326.1:p.Glu1164_His1165insGly
NM_139045.4:c.3666_3667insGGT NP_620614.2:p.Glu1222_His1223insGly