Canonical Allele Identifier: CA1417400182
Gene: SI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165046784A= , CM000665.2:g.165046784A= GRCh38
NC_000003.11:g.164764572A= , CM000665.1:g.164764572A= GRCh37
NC_000003.10:g.166247266A= NCBI36
NG_017043.1:g.36712T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264382.8:c.1887+57T= MANE Select ENSP00000264382.3:n.1887+57T=
ENST00000264382.7:c.1887+57T= ENSP00000264382.3:n.1887+57T=
NM_001041.3:c.1887+57T= NP_001032.2:n.1887+57T=
XM_011513078.1:c.1788+57T= XP_011511380.1:n.1788+57T=
XM_011513078.2:c.1788+57T= XP_011511380.1:n.1788+57T=
NM_001041.4:c.1887+57T= MANE Select NP_001032.2:n.1887+57T=
Search 100 bp 5'
Search 100 bp 3'