Canonical Allele Identifier: CA272661
Gene: STIL HGNC NCBI

Linked Data

ClinVar Variation Id: 160054
dbSNP Id: rs587784448

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.47280438_47280440del , CM000663.2:g.47280438_47280440del GRCh38
NC_000001.10:g.47746110_47746112del , CM000663.1:g.47746110_47746112del GRCh37
NC_000001.9:g.47518697_47518699del NCBI36
NG_012126.1:g.38711_38713del

Transcript Alleles

HGVS Amino-acid Change
ENST00000337817.10:c.1880_1882del ENSP00000337367.6:p.Cys627del
ENST00000436811.2:c.1513-74_1513-72del ENSP00000409087.2:n.1513-74_1513-72del
ENST00000447475.7:c.1880_1882del ENSP00000411664.3:p.Cys627del
ENST00000682940.1:n.648-74_648-72del
ENST00000682977.1:c.1880_1882del ENSP00000506981.1:p.Cys627del
ENST00000683977.1:c.1320_1322del
ENST00000684618.1:n.796_798del
ENST00000371877.8:c.2021_2023del MANE Select ENSP00000360944.3:p.Cys674del
ENST00000337817.9:c.1880_1882del ENSP00000337367.6:p.Cys627del
ENST00000360380.7:c.2021_2023del ENSP00000353544.3:p.Cys674del
ENST00000371877.7:c.2021_2023del ENSP00000360944.3:p.Cys674del
ENST00000396221.6:c.2021_2023del ENSP00000379523.2:p.Cys674del
ENST00000418131.1:n.2502_2504del
ENST00000436811.1:c.113-74_113-72del
ENST00000447475.6:c.1880_1882del ENSP00000411664.2:p.Cys627del
NM_001048166.1:c.2021_2023del MANE Select NP_001041631.1:p.Cys674del
NM_001282936.1:c.2021_2023del NP_001269865.1:p.Cys674del
NM_001282937.1:c.2021_2023del NP_001269866.1:p.Cys674del
NM_001282938.1:c.1880_1882del NP_001269867.1:p.Cys627del
NM_001282939.1:c.1880_1882del NP_001269868.1:p.Cys627del
NM_003035.2:c.2021_2023del NP_003026.2:p.Cys674del
XM_006710834.2:c.2021_2023del XP_006710897.1:p.Cys674del
XM_011541991.1:c.2021_2023del XP_011540293.1:p.Cys674del
XM_011541992.1:c.2021_2023del XP_011540294.1:p.Cys674del
XM_011541993.1:c.2021_2023del XP_011540295.1:p.Cys674del
XM_011541994.1:c.2021_2023del XP_011540296.1:p.Cys674del
XM_011541995.1:c.2021_2023del XP_011540297.1:p.Cys674del
XM_011541996.1:c.1880_1882del XP_011540298.1:p.Cys627del
XM_011541997.1:c.1880_1882del XP_011540299.1:p.Cys627del
XM_011541998.1:c.1880_1882del XP_011540300.1:p.Cys627del
XM_011541999.1:c.1325_1327del XP_011540301.1:p.Cys442del
XM_011542000.1:c.1325_1327del XP_011540302.1:p.Cys442del
XM_011542001.1:c.2021_2023del XP_011540303.1:p.Cys674del
XR_946746.1:n.2176_2178del
XM_006710834.3:c.2021_2023del XP_006710897.1:p.Cys674del
XM_011541991.2:c.2021_2023del XP_011540293.1:p.Cys674del
XM_011541992.2:c.2021_2023del XP_011540294.1:p.Cys674del
XM_011541994.2:c.2021_2023del XP_011540296.1:p.Cys674del
XM_011541996.2:c.1880_1882del XP_011540298.1:p.Cys627del
XM_011541998.2:c.1880_1882del XP_011540300.1:p.Cys627del
XM_011542001.2:c.2021_2023del XP_011540303.1:p.Cys674del
XM_017002123.1:c.1880_1882del XP_016857612.1:p.Cys627del
XM_017002124.1:c.1310_1312del XP_016857613.1:p.Cys437del
XM_017002125.1:c.2021_2023del XP_016857614.1:p.Cys674del
XM_017002126.1:c.2021_2023del XP_016857615.1:p.Cys674del
XM_017002127.1:c.2021_2023del XP_016857616.1:p.Cys674del
XR_001737370.1:n.2176_2178del
NM_001377417.1:c.1880_1882del NP_001364346.1:p.Cys627del