Canonical Allele Identifier: CA918396566
Gene: SMARCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1586721646

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2116033_2116034insATA , CM000671.2:g.2116033_2116034insATA GRCh38
NC_000009.11:g.2116033_2116034insATA , CM000671.1:g.2116033_2116034insATA GRCh37
NC_000009.10:g.2106033_2106034insATA NCBI36
NG_032162.1:g.105692_105693insATA
NG_032162.2:g.140744_140745insATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3308_3309insATA ENSP00000515861.1:p.His1103delinsGlnTyr
ENST00000704352.1:c.1174-45653_1174-45652insATA ENSP00000515863.1:n.1174-45653_1174-45652insATA
ENST00000704353.1:c.1174-45653_1174-45652insATA ENSP00000515864.1:n.1174-45653_1174-45652insATA
ENST00000704354.1:c.3652_3653insATA
ENST00000704355.1:c.2032_2033insATA
ENST00000349721.8:c.3668_3669insATA MANE Select ENSP00000265773.5:p.His1223delinsGlnTyr
ENST00000357248.8:c.3668_3669insATA ENSP00000349788.2:p.His1223delinsGlnTyr
ENST00000635739.1:n.2336_2337insATA
ENST00000636157.1:n.1275_1276insATA
ENST00000638139.1:n.702_703insATA
ENST00000349721.7:c.3668_3669insATA ENSP00000265773.5:p.His1223delinsGlnTyr
ENST00000357248.7:c.3668_3669insATA ENSP00000349788.2:p.His1223delinsGlnTyr
ENST00000382194.6:c.3668_3669insATA ENSP00000371629.1:p.His1223delinsGlnTyr
ENST00000382203.5:c.3668_3669insATA ENSP00000371638.1:p.His1223delinsGlnTyr
ENST00000450198.6:c.3494_3495insATA ENSP00000392081.2:p.His1165delinsGlnTyr
ENST00000634760.1:c.3668_3669insATA ENSP00000489256.1:p.His1223delinsGlnTyr
ENST00000634772.1:c.62-3425_62-3424insATA
ENST00000634925.1:n.1159_1160insATA
NM_001289396.1:c.3668_3669insATA NP_001276325.1:p.His1223delinsGlnTyr
NM_001289397.1:c.3494_3495insATA NP_001276326.1:p.His1165delinsGlnTyr
NM_003070.4:c.3668_3669insATA NP_003061.3:p.His1223delinsGlnTyr
NM_139045.3:c.3668_3669insATA NP_620614.2:p.His1223delinsGlnTyr
NM_003070.5:c.3668_3669insATA MANE Select NP_003061.3:p.His1223delinsGlnTyr
NM_001289397.2:c.3494_3495insATA NP_001276326.1:p.His1165delinsGlnTyr
NM_139045.4:c.3668_3669insATA NP_620614.2:p.His1223delinsGlnTyr