Canonical Allele Identifier: CA1327820243
Gene: SMARCAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216412607A= , CM000664.2:g.216412607A= GRCh38
NC_000002.11:g.217277330A= , CM000664.1:g.217277330A= GRCh37
NC_000002.10:g.216985575A= NCBI36
NG_009771.1:g.5194A= , LRG_108:g.5194A=

Transcript Alleles

HGVS Amino-acid change
ENST00000425815.6:c.-206A= ENSP00000394410.2:n.-206A=
ENST00000430374.6:c.-96+4A= ENSP00000405077.2:n.-96+4A=
ENST00000444508.6:c.-223A= ENSP00000398969.2:n.-223A=
ENST00000697898.1:n.225A=
ENST00000697899.1:c.-137A= ENSP00000513470.1:n.-137A=
ENST00000697900.1:n.140A=
ENST00000697901.1:c.-137A= ENSP00000513471.1:n.-137A=
ENST00000697902.1:n.96A=
ENST00000697903.1:c.-137A= ENSP00000513472.1:n.-137A=
ENST00000357276.9:c.-137A= MANE Select ENSP00000349823.4:n.-137A=
ENST00000357276.8:c.-137A= ENSP00000349823.4:n.-137A=
ENST00000425815.5:c.-206A= ENSP00000394410.1:n.-206A=
ENST00000430374.5:c.-96+4A= ENSP00000405077.1:n.-96+4A=
ENST00000444508.5:c.-223A= ENSP00000398969.1:n.-223A=
NM_014140.3:c.-137A= , LRG_108t1:c.-137A= NP_054859.2:n.-137A=
XM_005246631.2:c.-96+4A= XP_005246688.1:n.-96+4A=
XM_005246632.1:c.-223A= XP_005246689.1:n.-223A=
XM_006712557.1:c.-137A= XP_006712620.1:n.-137A=
XM_005246632.2:c.-223A= XP_005246689.1:n.-223A=
NM_014140.4:c.-137A= MANE Select NP_054859.2:n.-137A=