Canonical Allele Identifier: CA1327833014
Gene: SMARCAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216442014_216442016delinsTAG , CM000664.2:g.216442014_216442016delinsTAG GRCh38
NC_000002.11:g.217306737_217306739delinsTAG , CM000664.1:g.217306737_217306739delinsTAG GRCh37
NC_000002.10:g.217014982_217014984delinsTAG NCBI36
NG_009771.1:g.34601_34603delinsTAG , LRG_108:g.34601_34603delinsTAG

Transcript Alleles

HGVS Amino-acid change
ENST00000425815.6:c.1710+3529_1710+3531delinsTAG ENSP00000394410.2:n.1710+3529_1710+3531de...
ENST00000430374.6:c.1710+3529_1710+3531delinsTAG ENSP00000405077.2:n.1710+3529_1710+3531de...
ENST00000444508.6:c.1710+3529_1710+3531delinsTAG ENSP00000398969.2:n.1710+3529_1710+3531de...
ENST00000697898.1:n.2071+3529_2071+3531delinsTAG
ENST00000697899.1:c.1476+3529_1476+3531delinsTAG ENSP00000513470.1:n.1476+3529_1476+3531de...
ENST00000697901.1:c.*568+3529_*568+3531delinsTAG ENSP00000513471.1:n.*568+3529_*568+3531de...
ENST00000697902.1:n.1942+3529_1942+3531delinsTAG
ENST00000697903.1:c.*197+3529_*197+3531delinsTAG ENSP00000513472.1:n.*197+3529_*197+3531de...
ENST00000697904.1:c.*197+3529_*197+3531delinsTAG ENSP00000513473.1:n.*197+3529_*197+3531de...
ENST00000697905.1:c.*197+3529_*197+3531delinsTAG ENSP00000513474.1:n.*197+3529_*197+3531de...
ENST00000697906.1:c.1476+3529_1476+3531delinsTAG ENSP00000513475.1:n.1476+3529_1476+3531de...
ENST00000697907.1:c.*568+3529_*568+3531delinsTAG ENSP00000513476.1:n.*568+3529_*568+3531de...
ENST00000697908.1:n.1507+3529_1507+3531delinsTAG
ENST00000697909.1:n.602+3529_602+3531delinsTAG
ENST00000357276.9:c.1710+3529_1710+3531delinsTAG MANE Select ENSP00000349823.4:n.1710+3529_1710+3531de...
ENST00000357276.8:c.1710+3529_1710+3531delinsTAG ENSP00000349823.4:n.1710+3529_1710+3531de...
ENST00000358207.9:c.1710+3529_1710+3531delinsTAG ENSP00000350940.5:n.1710+3529_1710+3531de...
ENST00000392128.6:c.1237-5004_1237-5002delinsTAG ENSP00000375974.2:n.1237-5004_1237-5002de...
ENST00000445153.1:c.383+3529_383+3531delinsTAG
NM_001127207.1:c.1710+3529_1710+3531delinsTAG NP_001120679.1:n.1710+3529_1710+3531delin...
NM_014140.3:c.1710+3529_1710+3531delinsTAG , LRG_108t1:c.1710+3529_1710+3531delinsTAG NP_054859.2:n.1710+3529_1710+3531delinsTA...
XM_005246631.2:c.1710+3529_1710+3531delinsTAG XP_005246688.1:n.1710+3529_1710+3531delin...
XM_005246632.1:c.1710+3529_1710+3531delinsTAG XP_005246689.1:n.1710+3529_1710+3531delin...
XM_006712557.1:c.1645-5004_1645-5002delinsTAG XP_006712620.1:n.1645-5004_1645-5002delin...
XM_005246632.2:c.1710+3529_1710+3531delinsTAG XP_005246689.1:n.1710+3529_1710+3531delin...
XM_017004228.2:c.798+3529_798+3531delinsTAG XP_016859717.1:n.798+3529_798+3531delinsT...
NM_001127207.2:c.1710+3529_1710+3531delinsTAG NP_001120679.1:n.1710+3529_1710+3531delin...
NM_014140.4:c.1710+3529_1710+3531delinsTAG MANE Select NP_054859.2:n.1710+3529_1710+3531delinsTA...