Canonical Allele Identifier: CA1417381877
Gene: SI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165069004T= , CM000665.2:g.165069004T= GRCh38
NC_000003.11:g.164786792T= , CM000665.1:g.164786792T= GRCh37
NC_000003.10:g.166269486T= NCBI36
NG_017043.1:g.14492A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264382.8:c.373+74A= MANE Select ENSP00000264382.3:n.373+74A=
ENST00000264382.7:c.373+74A= ENSP00000264382.3:n.373+74A=
ENST00000476593.1:c.*248+74A= ENSP00000419450.1:n.*248+74A=
NM_001041.3:c.373+74A= NP_001032.2:n.373+74A=
XM_011513078.1:c.274+74A= XP_011511380.1:n.274+74A=
XM_011513078.2:c.274+74A= XP_011511380.1:n.274+74A=
NM_001041.4:c.373+74A= MANE Select NP_001032.2:n.373+74A=
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