Canonical Allele Identifier: CA1417400245

Gene: SI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165046845G= , CM000665.2:g.165046845G=	GRCh38
NC_000003.11:g.164764633G= , CM000665.1:g.164764633G=	GRCh37
NC_000003.10:g.166247327G=	NCBI36
NG_017043.1:g.36651C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264382.8:c.1883C= MANE Select	ENSP00000264382.3:p.Pro628=
ENST00000264382.7:c.1883C=	ENSP00000264382.3:p.Pro628=
NM_001041.3:c.1883C=	NP_001032.2:p.Pro628=
XM_011513078.1:c.1784C=	XP_011511380.1:p.Pro595=
XM_011513078.2:c.1784C=	XP_011511380.1:p.Pro595=
NM_001041.4:c.1883C= MANE Select	NP_001032.2:p.Pro628=