Canonical Allele Identifier: CA372789080

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2116026T>A (hg19) ; chr9:g.2116026T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2116026T>A , CM000671.2:g.2116026T>A	GRCh38
NC_000009.11:g.2116026T>A , CM000671.1:g.2116026T>A	GRCh37
NC_000009.10:g.2106026T>A	NCBI36
NG_032162.1:g.105685T>A
NG_032162.2:g.140737T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3301T>A	ENSP00000515861.1:p.Leu1101Met
ENST00000704352.1:c.1174-45660T>A	ENSP00000515863.1:n.1174-45660T>A
ENST00000704353.1:c.1174-45660T>A	ENSP00000515864.1:n.1174-45660T>A
ENST00000704354.1:c.3645T>A
ENST00000704355.1:c.2025T>A
ENST00000349721.8:c.3661T>A MANE Select	ENSP00000265773.5:p.Leu1221Met
ENST00000357248.8:c.3661T>A	ENSP00000349788.2:p.Leu1221Met
ENST00000635739.1:n.2329T>A
ENST00000636157.1:n.1268T>A
ENST00000638139.1:n.695T>A
ENST00000349721.7:c.3661T>A	ENSP00000265773.5:p.Leu1221Met
ENST00000357248.7:c.3661T>A	ENSP00000349788.2:p.Leu1221Met
ENST00000382194.6:c.3661T>A	ENSP00000371629.1:p.Leu1221Met
ENST00000382203.5:c.3661T>A	ENSP00000371638.1:p.Leu1221Met
ENST00000450198.6:c.3487T>A	ENSP00000392081.2:p.Leu1163Met
ENST00000634760.1:c.3661T>A	ENSP00000489256.1:p.Leu1221Met
ENST00000634772.1:c.62-3432T>A
ENST00000634925.1:n.1152T>A
NM_001289396.1:c.3661T>A	NP_001276325.1:p.Leu1221Met
NM_001289397.1:c.3487T>A	NP_001276326.1:p.Leu1163Met
NM_003070.4:c.3661T>A	NP_003061.3:p.Leu1221Met
NM_139045.3:c.3661T>A	NP_620614.2:p.Leu1221Met
NM_003070.5:c.3661T>A MANE Select	NP_003061.3:p.Leu1221Met
NM_001289397.2:c.3487T>A	NP_001276326.1:p.Leu1163Met
NM_139045.4:c.3661T>A	NP_620614.2:p.Leu1221Met