Canonical Allele Identifier: CA1327820245
Gene: SMARCAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216412615G= , CM000664.2:g.216412615G= GRCh38
NC_000002.11:g.217277338G= , CM000664.1:g.217277338G= GRCh37
NC_000002.10:g.216985583G= NCBI36
NG_009771.1:g.5202G= , LRG_108:g.5202G=

Transcript Alleles

HGVS Amino-acid change
ENST00000425815.6:c.-198G= ENSP00000394410.2:n.-198G=
ENST00000430374.6:c.-96+12G= ENSP00000405077.2:n.-96+12G=
ENST00000444508.6:c.-215G= ENSP00000398969.2:n.-215G=
ENST00000697898.1:n.233G=
ENST00000697899.1:c.-129G= ENSP00000513470.1:n.-129G=
ENST00000697900.1:n.148G=
ENST00000697901.1:c.-129G= ENSP00000513471.1:n.-129G=
ENST00000697902.1:n.104G=
ENST00000697903.1:c.-129G= ENSP00000513472.1:n.-129G=
ENST00000357276.9:c.-129G= MANE Select ENSP00000349823.4:n.-129G=
ENST00000357276.8:c.-129G= ENSP00000349823.4:n.-129G=
ENST00000425815.5:c.-198G= ENSP00000394410.1:n.-198G=
ENST00000430374.5:c.-96+12G= ENSP00000405077.1:n.-96+12G=
ENST00000444508.5:c.-215G= ENSP00000398969.1:n.-215G=
NM_014140.3:c.-129G= , LRG_108t1:c.-129G= NP_054859.2:n.-129G=
XM_005246631.2:c.-96+12G= XP_005246688.1:n.-96+12G=
XM_005246632.1:c.-215G= XP_005246689.1:n.-215G=
XM_006712557.1:c.-129G= XP_006712620.1:n.-129G=
XM_005246632.2:c.-215G= XP_005246689.1:n.-215G=
NM_014140.4:c.-129G= MANE Select NP_054859.2:n.-129G=