Canonical Allele Identifier: CA1417304019
Gene: SI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.164996805T= , CM000665.2:g.164996805T= GRCh38
NC_000003.11:g.164714593T= , CM000665.1:g.164714593T= GRCh37
NC_000003.10:g.166197287T= NCBI36
NG_017043.1:g.86691A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264382.8:c.4541-33A= MANE Select ENSP00000264382.3:n.4541-33A=
ENST00000264382.7:c.4541-33A= ENSP00000264382.3:n.4541-33A=
NM_001041.3:c.4541-33A= NP_001032.2:n.4541-33A=
XM_011513078.1:c.4442-33A= XP_011511380.1:n.4442-33A=
XM_011513078.2:c.4442-33A= XP_011511380.1:n.4442-33A=
NM_001041.4:c.4541-33A= MANE Select NP_001032.2:n.4541-33A=
Search 100 bp 5'
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