Canonical Allele Identifier: CA1327851092
Gene: SMARCAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216483024T= , CM000664.2:g.216483024T= GRCh38
NC_000002.11:g.217347747T= , CM000664.1:g.217347747T= GRCh37
NC_000002.10:g.217055992T= NCBI36
NG_009771.1:g.75611T= , LRG_108:g.75611T=

Transcript Alleles

HGVS Amino-acid change
ENST00000425815.6:c.*47T= ENSP00000394410.2:n.*47T=
ENST00000430374.6:c.*47T= ENSP00000405077.2:n.*47T=
ENST00000444508.6:c.*47T= ENSP00000398969.2:n.*47T=
ENST00000697899.1:c.*47T= ENSP00000513470.1:n.*47T=
ENST00000697903.1:c.*1399T= ENSP00000513472.1:n.*1399T=
ENST00000697904.1:c.*1399T= ENSP00000513473.1:n.*1399T=
ENST00000697905.1:c.*1399T= ENSP00000513474.1:n.*1399T=
ENST00000697906.1:c.*47T= ENSP00000513475.1:n.*47T=
ENST00000697907.1:c.*1770T= ENSP00000513476.1:n.*1770T=
ENST00000697909.1:n.1804T=
ENST00000697910.1:n.1309T=
ENST00000357276.9:c.*47T= MANE Select ENSP00000349823.4:n.*47T=
ENST00000357276.8:c.*47T= ENSP00000349823.4:n.*47T=
NM_001127207.1:c.*47T= NP_001120679.1:n.*47T=
NM_014140.3:c.*47T= , LRG_108t1:c.*47T= NP_054859.2:n.*47T=
XM_005246631.2:c.*47T= XP_005246688.1:n.*47T=
XM_005246632.1:c.*47T= XP_005246689.1:n.*47T=
XM_006712557.1:c.*47T= XP_006712620.1:n.*47T=
XM_005246632.2:c.*47T= XP_005246689.1:n.*47T=
XM_017004228.2:c.*47T= XP_016859717.1:n.*47T=
NM_001127207.2:c.*47T= NP_001120679.1:n.*47T=
NM_014140.4:c.*47T= MANE Select NP_054859.2:n.*47T=