Canonical Allele Identifier: CA355052177
Gene: SI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165046900C>A , CM000665.2:g.165046900C>A GRCh38
NC_000003.11:g.164764688C>A , CM000665.1:g.164764688C>A GRCh37
NC_000003.10:g.166247382C>A NCBI36
NG_017043.1:g.36596G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264382.8:c.1828G>T MANE Select ENSP00000264382.3:p.Glu610Ter
ENST00000264382.7:c.1828G>T ENSP00000264382.3:p.Glu610Ter
NM_001041.3:c.1828G>T NP_001032.2:p.Glu610Ter
XM_011513078.1:c.1729G>T XP_011511380.1:p.Glu577Ter
XM_011513078.2:c.1729G>T XP_011511380.1:p.Glu577Ter
NM_001041.4:c.1828G>T MANE Select NP_001032.2:p.Glu610Ter