Canonical Allele Identifier: CA2668418787
Gene: SI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.164996797_164996800del , CM000665.2:g.164996797_164996800del GRCh38
NC_000003.11:g.164714585_164714588del , CM000665.1:g.164714585_164714588del GRCh37
NC_000003.10:g.166197279_166197282del NCBI36
NG_017043.1:g.86696_86699del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264382.8:c.4541-28_4541-25del MANE Select ENSP00000264382.3:n.4541-28_4541-25del
ENST00000264382.7:c.4541-28_4541-25del ENSP00000264382.3:n.4541-28_4541-25del
NM_001041.3:c.4541-28_4541-25del NP_001032.2:n.4541-28_4541-25del
XM_011513078.1:c.4442-28_4442-25del XP_011511380.1:n.4442-28_4442-25del
XM_011513078.2:c.4442-28_4442-25del XP_011511380.1:n.4442-28_4442-25del
NM_001041.4:c.4541-28_4541-25del MANE Select NP_001032.2:n.4541-28_4541-25del