Canonical Allele Identifier: CA1327827162
Gene: SMARCAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216428631_216428642delinsGACCCTCTGCCC , CM000664.2:g.216428631_216428642delinsGACCCTCTGCCC GRCh38
NC_000002.11:g.217293354_217293365delinsGACCCTCTGCCC , CM000664.1:g.217293354_217293365delinsGACCCTCTGCCC GRCh37
NC_000002.10:g.217001599_217001610delinsGACCCTCTGCCC NCBI36
NG_009771.1:g.21218_21229delinsGACCCTCTGCCC , LRG_108:g.21218_21229delinsGACCCTCTGCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000425815.6:c.1183_1194delinsGACCCTCTGCCC ENSP00000394410.2:p.Asp395=
ENST00000430374.6:c.1183_1194delinsGACCCTCTGCCC ENSP00000405077.2:p.Asp395=
ENST00000444508.6:c.1183_1194delinsGACCCTCTGCCC ENSP00000398969.2:p.Asp395=
ENST00000697898.1:n.1544_1555delinsGACCCTCTGCCC
ENST00000697899.1:c.949_960delinsGACCCTCTGCCC ENSP00000513470.1:p.Asp317=
ENST00000697900.1:n.1459_1470delinsGACCCTCTGCCC
ENST00000697901.1:c.*41_*52delinsGACCCTCTGCCC ENSP00000513471.1:n.*41_*52delinsGACCCTCT...
ENST00000697902.1:n.1415_1426delinsGACCCTCTGCCC
ENST00000697903.1:c.1183_1194delinsGACCCTCTGCCC ENSP00000513472.1:p.Asp395=
ENST00000697904.1:c.1183_1194delinsGACCCTCTGCCC ENSP00000513473.1:p.Asp395=
ENST00000697905.1:c.1183_1194delinsGACCCTCTGCCC ENSP00000513474.1:p.Asp395=
ENST00000697906.1:c.949_960delinsGACCCTCTGCCC ENSP00000513475.1:p.Asp317=
ENST00000697907.1:c.*41_*52delinsGACCCTCTGCCC ENSP00000513476.1:n.*41_*52delinsGACCCTCT...
ENST00000697908.1:n.980_991delinsGACCCTCTGCCC
ENST00000357276.9:c.1183_1194delinsGACCCTCTGCCC MANE Select ENSP00000349823.4:p.Asp395=
ENST00000357276.8:c.1183_1194delinsGACCCTCTGCCC ENSP00000349823.4:p.Asp395=
ENST00000358207.9:c.1183_1194delinsGACCCTCTGCCC ENSP00000350940.5:p.Asp395=
ENST00000392128.6:c.775_786delinsGACCCTCTGCCC ENSP00000375974.2:p.Asp259=
ENST00000412913.1:c.343_354delinsGACCCTCTGCCC ENSP00000390248.1:p.Asp115=
ENST00000427645.5:c.829_840delinsGACCCTCTGCCC ENSP00000392997.1:p.Asp277=
ENST00000479008.1:n.427_438delinsGACCCTCTGCCC
NM_001127207.1:c.1183_1194delinsGACCCTCTGCCC NP_001120679.1:p.Asp395=
NM_014140.3:c.1183_1194delinsGACCCTCTGCCC , LRG_108t1:c.1183_1194delinsGACCCTCTGCCC NP_054859.2:p.Asp395=
XM_005246631.2:c.1183_1194delinsGACCCTCTGCCC XP_005246688.1:p.Asp395=
XM_005246632.1:c.1183_1194delinsGACCCTCTGCCC XP_005246689.1:p.Asp395=
XM_006712557.1:c.1183_1194delinsGACCCTCTGCCC XP_006712620.1:p.Asp395=
XM_005246632.2:c.1183_1194delinsGACCCTCTGCCC XP_005246689.1:p.Asp395=
XM_017004228.2:c.271_282delinsGACCCTCTGCCC XP_016859717.1:p.Asp91=
NM_001127207.2:c.1183_1194delinsGACCCTCTGCCC NP_001120679.1:p.Asp395=
NM_014140.4:c.1183_1194delinsGACCCTCTGCCC MANE Select NP_054859.2:p.Asp395=