Canonical Allele Identifier: CA1417400076

Gene: SI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165046675T= , CM000665.2:g.165046675T=	GRCh38
NC_000003.11:g.164764463T= , CM000665.1:g.164764463T=	GRCh37
NC_000003.10:g.166247157T=	NCBI36
NG_017043.1:g.36821A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264382.8:c.1887+166A= MANE Select	ENSP00000264382.3:n.1887+166A=
ENST00000264382.7:c.1887+166A=	ENSP00000264382.3:n.1887+166A=
NM_001041.3:c.1887+166A=	NP_001032.2:n.1887+166A=
XM_011513078.1:c.1788+166A=	XP_011511380.1:n.1788+166A=
XM_011513078.2:c.1788+166A=	XP_011511380.1:n.1788+166A=
NM_001041.4:c.1887+166A= MANE Select	NP_001032.2:n.1887+166A=