Canonical Allele Identifier: CA2637750006

Gene: SMARCE1

Linked Data

• gnomAD v4: 17-40628450-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40628450C>T , CM000679.2:g.40628450C>T	GRCh38
NC_000017.10:g.38784702C>T , CM000679.1:g.38784702C>T	GRCh37
NC_000017.9:g.36038228C>T	NCBI36
NG_032163.1:g.24402G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264640.9:c.*1133G>A	ENSP00000466608.2:n.*1133G>A
ENST00000348513.12:c.*335G>A MANE Select	ENSP00000323967.6:n.*335G>A
ENST00000377808.9:c.*558G>A	ENSP00000367039.4:n.*558G>A
ENST00000400122.8:c.*558G>A	ENSP00000411607.2:n.*558G>A
ENST00000469334.6:n.2169G>A
ENST00000578112.6:c.*1368G>A	ENSP00000464501.1:n.*1368G>A
ENST00000580419.6:c.*550G>A	ENSP00000462475.2:n.*550G>A
ENST00000642576.1:n.2714G>A
ENST00000643030.1:n.2194G>A
ENST00000643255.1:c.*3635G>A	ENSP00000493957.1:n.*3635G>A
ENST00000643318.1:c.*335G>A	ENSP00000494771.1:n.*335G>A
ENST00000643378.1:n.2126G>A
ENST00000643683.1:c.*335G>A	ENSP00000496094.1:n.*335G>A
ENST00000643893.1:n.1864G>A
ENST00000644443.1:n.3459G>A
ENST00000644523.1:n.1617G>A
ENST00000644527.1:c.*335G>A	ENSP00000493974.1:n.*335G>A
ENST00000644701.1:c.*558G>A	ENSP00000496097.1:n.*558G>A
ENST00000644909.1:c.*840G>A	ENSP00000493649.1:n.*840G>A
ENST00000645152.1:n.2234G>A
ENST00000645227.1:c.*1259G>A	ENSP00000495021.1:n.*1259G>A
ENST00000646242.1:n.7483G>A
ENST00000646283.1:c.*335G>A	ENSP00000494537.1:n.*335G>A
ENST00000646401.1:n.2937G>A
ENST00000646856.1:c.*1447G>A	ENSP00000494505.1:n.*1447G>A
ENST00000647294.1:c.*1501G>A	ENSP00000494815.1:n.*1501G>A
ENST00000647508.1:c.*335G>A	ENSP00000496445.1:n.*335G>A
ENST00000647515.1:c.*1102G>A	ENSP00000495857.1:n.*1102G>A
ENST00000348513.10:c.*335G>A	ENSP00000323967.6:n.*335G>A
ENST00000578112.5:c.*1368G>A	ENSP00000464501.1:n.*1368G>A
NM_003079.4:c.*335G>A	NP_003070.3:n.*335G>A
NM_003079.5:c.*335G>A MANE Select	NP_003070.3:n.*335G>A