Canonical Allele Identifier: CA1327848696
Gene: SMARCAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216477051A= , CM000664.2:g.216477051A= GRCh38
NC_000002.11:g.217341774A= , CM000664.1:g.217341774A= GRCh37
NC_000002.10:g.217050019A= NCBI36
NG_009771.1:g.69638A= , LRG_108:g.69638A=

Transcript Alleles

HGVS Amino-acid change
ENST00000425815.6:c.2428-58A= ENSP00000394410.2:n.2428-58A=
ENST00000430374.6:c.2428-58A= ENSP00000405077.2:n.2428-58A=
ENST00000444508.6:c.2428-58A= ENSP00000398969.2:n.2428-58A=
ENST00000697899.1:c.2194-58A= ENSP00000513470.1:n.2194-58A=
ENST00000697901.1:c.*1183-58A= ENSP00000513471.1:n.*1183-58A=
ENST00000697903.1:c.*915-58A= ENSP00000513472.1:n.*915-58A=
ENST00000697904.1:c.*915-58A= ENSP00000513473.1:n.*915-58A=
ENST00000697905.1:c.*915-58A= ENSP00000513474.1:n.*915-58A=
ENST00000697906.1:c.2194-58A= ENSP00000513475.1:n.2194-58A=
ENST00000697907.1:c.*1286-58A= ENSP00000513476.1:n.*1286-58A=
ENST00000697908.1:n.2122-58A=
ENST00000697909.1:n.1320-58A=
ENST00000697910.1:n.825-58A=
ENST00000697911.1:n.734-58A=
ENST00000357276.9:c.2428-58A= MANE Select ENSP00000349823.4:n.2428-58A=
ENST00000357276.8:c.2428-58A= ENSP00000349823.4:n.2428-58A=
ENST00000358207.9:c.2428-58A= ENSP00000350940.5:n.2428-58A=
ENST00000392128.6:c.1954-58A= ENSP00000375974.2:n.1954-58A=
NM_001127207.1:c.2428-58A= NP_001120679.1:n.2428-58A=
NM_014140.3:c.2428-58A= , LRG_108t1:c.2428-58A= NP_054859.2:n.2428-58A=
XM_005246631.2:c.2428-58A= XP_005246688.1:n.2428-58A=
XM_005246632.1:c.2428-58A= XP_005246689.1:n.2428-58A=
XM_006712557.1:c.2362-58A= XP_006712620.1:n.2362-58A=
XM_005246632.2:c.2428-58A= XP_005246689.1:n.2428-58A=
XM_017004228.2:c.1516-58A= XP_016859717.1:n.1516-58A=
NM_001127207.2:c.2428-58A= NP_001120679.1:n.2428-58A=
NM_014140.4:c.2428-58A= MANE Select NP_054859.2:n.2428-58A=