Canonical Allele Identifier: CA2675501382
Gene: SIL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946800_138946805del , CM000667.2:g.138946800_138946805del GRCh38
NC_000005.9:g.138282489_138282494del , CM000667.1:g.138282489_138282494del GRCh37
NC_000005.8:g.138310388_138310393del NCBI36
NG_008112.1:g.256574_256579del
NG_008112.2:g.256574_256579del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*314_*319del MANE Select ENSP00000378294.2:n.*314_*319del
ENST00000265195.9:c.*314_*319del ENSP00000265195.5:n.*314_*319del
ENST00000394817.6:c.*314_*319del ENSP00000378294.2:n.*314_*319del
NM_001037633.1:c.*314_*319del NP_001032722.1:n.*314_*319del
NM_022464.4:c.*314_*319del NP_071909.1:n.*314_*319del
XM_011543570.2:c.*314_*319del XP_011541872.1:n.*314_*319del
XM_024446164.1:c.*314_*319del XP_024301932.1:n.*314_*319del
NM_022464.5:c.*314_*319del MANE Select NP_071909.1:n.*314_*319del
NM_001037633.2:c.*314_*319del NP_001032722.1:n.*314_*319del