Canonical Allele Identifier: CA372788745
Gene: SMARCA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2115876G>T , CM000671.2:g.2115876G>T GRCh38
NC_000009.11:g.2115876G>T , CM000671.1:g.2115876G>T GRCh37
NC_000009.10:g.2105876G>T NCBI36
NG_032162.1:g.105535G>T
NG_032162.2:g.140587G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3151G>T ENSP00000515861.1:p.Val1051Leu
ENST00000704352.1:c.1174-45810G>T ENSP00000515863.1:n.1174-45810G>T
ENST00000704353.1:c.1174-45810G>T ENSP00000515864.1:n.1174-45810G>T
ENST00000704354.1:c.3495G>T
ENST00000704355.1:c.1875G>T
ENST00000349721.8:c.3511G>T MANE Select ENSP00000265773.5:p.Val1171Leu
ENST00000357248.8:c.3511G>T ENSP00000349788.2:p.Val1171Leu
ENST00000635739.1:n.2179G>T
ENST00000636157.1:n.1118G>T
ENST00000638139.1:n.545G>T
ENST00000349721.7:c.3511G>T ENSP00000265773.5:p.Val1171Leu
ENST00000357248.7:c.3511G>T ENSP00000349788.2:p.Val1171Leu
ENST00000382194.6:c.3511G>T ENSP00000371629.1:p.Val1171Leu
ENST00000382203.5:c.3511G>T ENSP00000371638.1:p.Val1171Leu
ENST00000450198.6:c.3337G>T ENSP00000392081.2:p.Val1113Leu
ENST00000634760.1:c.3511G>T ENSP00000489256.1:p.Val1171Leu
ENST00000634772.1:c.62-3582G>T
ENST00000634925.1:n.1002G>T
NM_001289396.1:c.3511G>T NP_001276325.1:p.Val1171Leu
NM_001289397.1:c.3337G>T NP_001276326.1:p.Val1113Leu
NM_003070.4:c.3511G>T NP_003061.3:p.Val1171Leu
NM_139045.3:c.3511G>T NP_620614.2:p.Val1171Leu
NM_003070.5:c.3511G>T MANE Select NP_003061.3:p.Val1171Leu
NM_001289397.2:c.3337G>T NP_001276326.1:p.Val1113Leu
NM_139045.4:c.3511G>T NP_620614.2:p.Val1171Leu