Canonical Allele Identifier: CA372792626

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2191295A>G (hg19) ; chr9:g.2191295A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2191295A>G , CM000671.2:g.2191295A>G	GRCh38
NC_000009.11:g.2191295A>G , CM000671.1:g.2191295A>G	GRCh37
NC_000009.10:g.2181295A>G	NCBI36
NG_032162.1:g.180954A>G
NG_032162.2:g.216006A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.4210A>G	ENSP00000515861.1:p.Asn1404Asp
ENST00000704352.1:c.1762A>G	ENSP00000515863.1:p.Asn588Asp
ENST00000704353.1:c.1816A>G	ENSP00000515864.1:p.Asn606Asp
ENST00000704354.1:c.4554A>G
ENST00000704355.1:c.2934A>G
ENST00000349721.8:c.4624A>G MANE Select	ENSP00000265773.5:p.Asn1542Asp
ENST00000357248.8:c.4570A>G	ENSP00000349788.2:p.Asn1524Asp
ENST00000635739.1:n.3238A>G
ENST00000636157.1:n.2177A>G
ENST00000636367.1:c.*420A>G	ENSP00000489942.1:n.*420A>G
ENST00000638139.1:n.1658A>G
ENST00000639760.2:c.677A>G
ENST00000302401.8:c.688A>G	ENSP00000305411.3:p.Asn230Asp
ENST00000324954.10:c.598A>G	ENSP00000324770.6:p.Asn200Asp
ENST00000349721.7:c.4624A>G	ENSP00000265773.5:p.Asn1542Asp
ENST00000357248.7:c.4570A>G	ENSP00000349788.2:p.Asn1524Asp
ENST00000382183.6:c.562A>G	ENSP00000371618.1:p.Asn188Asp
ENST00000382185.6:c.682A>G	ENSP00000371620.2:p.Asn228Asp
ENST00000382186.6:c.616A>G	ENSP00000371621.1:p.Asn206Asp
ENST00000382194.6:c.4570A>G	ENSP00000371629.1:p.Asn1524Asp
ENST00000382203.5:c.4624A>G	ENSP00000371638.1:p.Asn1542Asp
ENST00000416751.2:c.562A>G	ENSP00000412242.2:p.Asn188Asp
ENST00000417599.6:c.682A>G	ENSP00000387486.2:p.Asn228Asp
ENST00000423555.6:c.682A>G	ENSP00000413057.2:p.Asn228Asp
ENST00000450198.6:c.4396A>G	ENSP00000392081.2:p.Asn1466Asp
ENST00000634760.1:c.*231A>G	ENSP00000489256.1:n.*231A>G
ENST00000634781.1:c.634A>G	ENSP00000489302.1:p.Asn212Asp
ENST00000634931.1:c.616A>G	ENSP00000489433.1:p.Asn206Asp
ENST00000634989.1:c.*420A>G	ENSP00000489100.1:n.*420A>G
ENST00000635273.1:n.466A>G
ENST00000635388.1:c.562A>G	ENSP00000489271.1:p.Asn188Asp
ENST00000635530.1:c.682A>G	ENSP00000489204.1:p.Asn228Asp
ENST00000635590.1:c.*420A>G	ENSP00000489587.1:n.*420A>G
ENST00000635659.1:c.715A>G
NM_001289396.1:c.4624A>G	NP_001276325.1:p.Asn1542Asp
NM_001289397.1:c.4396A>G	NP_001276326.1:p.Asn1466Asp
NM_001289398.1:c.598A>G	NP_001276327.1:p.Asn200Asp
NM_001289399.1:c.682A>G	NP_001276328.1:p.Asn228Asp
NM_001289400.1:c.688A>G	NP_001276329.1:p.Asn230Asp
NM_003070.4:c.4624A>G	NP_003061.3:p.Asn1542Asp
NM_139045.3:c.4570A>G	NP_620614.2:p.Asn1524Asp
XR_001746600.1:n.1362-10273T>C
XR_001746601.1:n.1316-10273T>C
NM_003070.5:c.4624A>G MANE Select	NP_003061.3:p.Asn1542Asp
NM_001289397.2:c.4396A>G	NP_001276326.1:p.Asn1466Asp
NM_001289398.2:c.598A>G	NP_001276327.1:p.Asn200Asp
NM_139045.4:c.4570A>G	NP_620614.2:p.Asn1524Asp