Canonical Allele Identifier: CA463711863

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2191324A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2191324A>G , CM000671.2:g.2191324A>G	GRCh38
NC_000009.11:g.2191324A>G , CM000671.1:g.2191324A>G	GRCh37
NC_000009.10:g.2181324A>G	NCBI36
NG_032162.1:g.180983A>G
NG_032162.2:g.216035A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.4239A>G	ENSP00000515861.1:p.Lys1413=
ENST00000704352.1:c.1791A>G	ENSP00000515863.1:p.Lys597=
ENST00000704353.1:c.1845A>G	ENSP00000515864.1:p.Lys615=
ENST00000704354.1:c.4583A>G
ENST00000704355.1:c.2963A>G
ENST00000349721.8:c.4653A>G MANE Select	ENSP00000265773.5:p.Lys1551=
ENST00000357248.8:c.4599A>G	ENSP00000349788.2:p.Lys1533=
ENST00000635739.1:n.3267A>G
ENST00000636157.1:n.2206A>G
ENST00000636367.1:c.*449A>G	ENSP00000489942.1:n.*449A>G
ENST00000638139.1:n.1687A>G
ENST00000639760.2:c.706A>G
ENST00000302401.8:c.717A>G	ENSP00000305411.3:p.Lys239=
ENST00000324954.10:c.627A>G	ENSP00000324770.6:p.Lys209=
ENST00000349721.7:c.4653A>G	ENSP00000265773.5:p.Lys1551=
ENST00000357248.7:c.4599A>G	ENSP00000349788.2:p.Lys1533=
ENST00000382183.6:c.591A>G	ENSP00000371618.1:p.Lys197=
ENST00000382185.6:c.711A>G	ENSP00000371620.2:p.Lys237=
ENST00000382186.6:c.645A>G	ENSP00000371621.1:p.Lys215=
ENST00000382194.6:c.4599A>G	ENSP00000371629.1:p.Lys1533=
ENST00000382203.5:c.4653A>G	ENSP00000371638.1:p.Lys1551=
ENST00000417599.6:c.711A>G	ENSP00000387486.2:p.Lys237=
ENST00000450198.6:c.4425A>G	ENSP00000392081.2:p.Lys1475=
ENST00000634760.1:c.*260A>G	ENSP00000489256.1:n.*260A>G
ENST00000634781.1:c.663A>G	ENSP00000489302.1:p.Lys221=
ENST00000634931.1:c.645A>G	ENSP00000489433.1:p.Lys215=
ENST00000634989.1:c.*449A>G	ENSP00000489100.1:n.*449A>G
ENST00000635273.1:n.495A>G
ENST00000635388.1:c.591A>G	ENSP00000489271.1:p.Lys197=
ENST00000635590.1:c.*449A>G	ENSP00000489587.1:n.*449A>G
ENST00000635659.1:c.744A>G
NM_001289396.1:c.4653A>G	NP_001276325.1:p.Lys1551=
NM_001289397.1:c.4425A>G	NP_001276326.1:p.Lys1475=
NM_001289398.1:c.627A>G	NP_001276327.1:p.Lys209=
NM_001289399.1:c.711A>G	NP_001276328.1:p.Lys237=
NM_001289400.1:c.717A>G	NP_001276329.1:p.Lys239=
NM_003070.4:c.4653A>G	NP_003061.3:p.Lys1551=
NM_139045.3:c.4599A>G	NP_620614.2:p.Lys1533=
XR_001746600.1:n.1362-10302T>C
XR_001746601.1:n.1316-10302T>C
NM_003070.5:c.4653A>G MANE Select	NP_003061.3:p.Lys1551=
NM_001289397.2:c.4425A>G	NP_001276326.1:p.Lys1475=
NM_001289398.2:c.627A>G	NP_001276327.1:p.Lys209=
NM_139045.4:c.4599A>G	NP_620614.2:p.Lys1533=