Canonical Allele Identifier: CA1327851090
Gene: SMARCAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216483020G= , CM000664.2:g.216483020G= GRCh38
NC_000002.11:g.217347743G= , CM000664.1:g.217347743G= GRCh37
NC_000002.10:g.217055988G= NCBI36
NG_009771.1:g.75607G= , LRG_108:g.75607G=

Transcript Alleles

HGVS Amino-acid change
ENST00000425815.6:c.*43G= ENSP00000394410.2:n.*43G=
ENST00000430374.6:c.*43G= ENSP00000405077.2:n.*43G=
ENST00000444508.6:c.*43G= ENSP00000398969.2:n.*43G=
ENST00000697899.1:c.*43G= ENSP00000513470.1:n.*43G=
ENST00000697903.1:c.*1395G= ENSP00000513472.1:n.*1395G=
ENST00000697904.1:c.*1395G= ENSP00000513473.1:n.*1395G=
ENST00000697905.1:c.*1395G= ENSP00000513474.1:n.*1395G=
ENST00000697906.1:c.*43G= ENSP00000513475.1:n.*43G=
ENST00000697907.1:c.*1766G= ENSP00000513476.1:n.*1766G=
ENST00000697909.1:n.1800G=
ENST00000697910.1:n.1305G=
ENST00000357276.9:c.*43G= MANE Select ENSP00000349823.4:n.*43G=
ENST00000357276.8:c.*43G= ENSP00000349823.4:n.*43G=
NM_001127207.1:c.*43G= NP_001120679.1:n.*43G=
NM_014140.3:c.*43G= , LRG_108t1:c.*43G= NP_054859.2:n.*43G=
XM_005246631.2:c.*43G= XP_005246688.1:n.*43G=
XM_005246632.1:c.*43G= XP_005246689.1:n.*43G=
XM_006712557.1:c.*43G= XP_006712620.1:n.*43G=
XM_005246632.2:c.*43G= XP_005246689.1:n.*43G=
XM_017004228.2:c.*43G= XP_016859717.1:n.*43G=
NM_001127207.2:c.*43G= NP_001120679.1:n.*43G=
NM_014140.4:c.*43G= MANE Select NP_054859.2:n.*43G=