Canonical Allele Identifier: CA1417400353

Gene: SI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165046911G= , CM000665.2:g.165046911G=	GRCh38
NC_000003.11:g.164764699G= , CM000665.1:g.164764699G=	GRCh37
NC_000003.10:g.166247393G=	NCBI36
NG_017043.1:g.36585C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264382.8:c.1817C= MANE Select	ENSP00000264382.3:p.Thr606=
ENST00000264382.7:c.1817C=	ENSP00000264382.3:p.Thr606=
NM_001041.3:c.1817C=	NP_001032.2:p.Thr606=
XM_011513078.1:c.1718C=	XP_011511380.1:p.Thr573=
XM_011513078.2:c.1718C=	XP_011511380.1:p.Thr573=
NM_001041.4:c.1817C= MANE Select	NP_001032.2:p.Thr606=