Canonical Allele Identifier: CA2782667831

Gene: SMARCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2116146_2116147insACT , CM000671.2:g.2116146_2116147insACT	GRCh38
NC_000009.11:g.2116146_2116147insACT , CM000671.1:g.2116146_2116147insACT	GRCh37
NC_000009.10:g.2106146_2106147insACT	NCBI36
NG_032162.1:g.105805_105806insACT
NG_032162.2:g.140857_140858insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3324+97_3324+98insACT	ENSP00000515861.1:n.3324+97_3324+98insACT
ENST00000704352.1:c.1174-45540_1174-45539insACT	ENSP00000515863.1:n.1174-45540_1174-45539insACT
ENST00000704353.1:c.1174-45540_1174-45539insACT	ENSP00000515864.1:n.1174-45540_1174-45539insACT
ENST00000704354.1:c.3668+97_3668+98insACT
ENST00000704355.1:c.2048+97_2048+98insACT
ENST00000349721.8:c.3684+97_3684+98insACT MANE Select	ENSP00000265773.5:n.3684+97_3684+98insACT
ENST00000357248.8:c.3684+97_3684+98insACT	ENSP00000349788.2:n.3684+97_3684+98insACT
ENST00000635739.1:n.2352+97_2352+98insACT
ENST00000636157.1:n.1291+97_1291+98insACT
ENST00000638139.1:n.718+97_718+98insACT
ENST00000349721.7:c.3684+97_3684+98insACT	ENSP00000265773.5:n.3684+97_3684+98insACT
ENST00000357248.7:c.3684+97_3684+98insACT	ENSP00000349788.2:n.3684+97_3684+98insACT
ENST00000382194.6:c.3684+97_3684+98insACT	ENSP00000371629.1:n.3684+97_3684+98insACT
ENST00000382203.5:c.3684+97_3684+98insACT	ENSP00000371638.1:n.3684+97_3684+98insACT
ENST00000450198.6:c.3510+97_3510+98insACT	ENSP00000392081.2:n.3510+97_3510+98insACT
ENST00000634760.1:c.3684+97_3684+98insACT	ENSP00000489256.1:n.3684+97_3684+98insACT
ENST00000634772.1:c.62-3312_62-3311insACT
ENST00000634925.1:n.1175+97_1175+98insACT
NM_001289396.1:c.3684+97_3684+98insACT	NP_001276325.1:n.3684+97_3684+98insACT
NM_001289397.1:c.3510+97_3510+98insACT	NP_001276326.1:n.3510+97_3510+98insACT
NM_003070.4:c.3684+97_3684+98insACT	NP_003061.3:n.3684+97_3684+98insACT
NM_139045.3:c.3684+97_3684+98insACT	NP_620614.2:n.3684+97_3684+98insACT
NM_003070.5:c.3684+97_3684+98insACT MANE Select	NP_003061.3:n.3684+97_3684+98insACT
NM_001289397.2:c.3510+97_3510+98insACT	NP_001276326.1:n.3510+97_3510+98insACT
NM_139045.4:c.3684+97_3684+98insACT	NP_620614.2:n.3684+97_3684+98insACT