Canonical Allele Identifier: CA1417400202

Gene: SI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165046802_165046803delinsTG , CM000665.2:g.165046802_165046803delinsTG	GRCh38
NC_000003.11:g.164764590_164764591delinsTG , CM000665.1:g.164764590_164764591delinsTG	GRCh37
NC_000003.10:g.166247284_166247285delinsTG	NCBI36
NG_017043.1:g.36693_36694delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264382.8:c.1887+38_1887+39delinsCA MANE Select	ENSP00000264382.3:n.1887+38_1887+39delinsCA
ENST00000264382.7:c.1887+38_1887+39delinsCA	ENSP00000264382.3:n.1887+38_1887+39delinsCA
NM_001041.3:c.1887+38_1887+39delinsCA	NP_001032.2:n.1887+38_1887+39delinsCA
XM_011513078.1:c.1788+38_1788+39delinsCA	XP_011511380.1:n.1788+38_1788+39delinsCA
XM_011513078.2:c.1788+38_1788+39delinsCA	XP_011511380.1:n.1788+38_1788+39delinsCA
NM_001041.4:c.1887+38_1887+39delinsCA MANE Select	NP_001032.2:n.1887+38_1887+39delinsCA