Canonical Allele Identifier: CA1417400251

Gene: SI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165046850T= , CM000665.2:g.165046850T=	GRCh38
NC_000003.11:g.164764638T= , CM000665.1:g.164764638T=	GRCh37
NC_000003.10:g.166247332T=	NCBI36
NG_017043.1:g.36646A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264382.8:c.1878A= MANE Select	ENSP00000264382.3:p.Gly626=
ENST00000264382.7:c.1878A=	ENSP00000264382.3:p.Gly626=
NM_001041.3:c.1878A=	NP_001032.2:p.Gly626=
XM_011513078.1:c.1779A=	XP_011511380.1:p.Gly593=
XM_011513078.2:c.1779A=	XP_011511380.1:p.Gly593=
NM_001041.4:c.1878A= MANE Select	NP_001032.2:p.Gly626=