Canonical Allele Identifier: CA354642018

Gene: STAG1

Linked Data

• dbSNP Id: rs1936343493
• MyVariant Identifiers: chr3:g.136068009G>A (hg19) ; chr3:g.136349167G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136349167G>A , CM000665.2:g.136349167G>A	GRCh38
NC_000003.11:g.136068009G>A , CM000665.1:g.136068009G>A	GRCh37
NC_000003.10:g.137550699G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383202.7:c.3262C>T MANE Select	ENSP00000372689.2:p.Arg1088Ter
ENST00000236698.9:c.3262C>T	ENSP00000236698.5:p.Arg1088Ter
ENST00000383202.6:c.3262C>T	ENSP00000372689.2:p.Arg1088Ter
ENST00000434713.6:c.2482C>T	ENSP00000404396.2:p.Arg828Ter
ENST00000465961.1:n.368C>T
ENST00000483235.5:c.*3252C>T	ENSP00000419093.1:n.*3252C>T
ENST00000629124.2:c.*2901C>T	ENSP00000486745.1:n.*2901C>T
NM_005862.2:c.3262C>T	NP_005853.2:p.Arg1088Ter
XM_011512329.1:c.2851C>T	XP_011510631.1:p.Arg951Ter
XM_011512330.1:c.2851C>T	XP_011510632.1:p.Arg951Ter
XM_011512331.1:c.2851C>T	XP_011510633.1:p.Arg951Ter
XM_011512332.1:c.2584C>T	XP_011510634.1:p.Arg862Ter
XM_011512333.1:c.2851C>T	XP_011510635.1:p.Arg951Ter
XM_011512329.2:c.2851C>T	XP_011510631.1:p.Arg951Ter
XM_011512331.2:c.2851C>T	XP_011510633.1:p.Arg951Ter
XM_017005523.1:c.2851C>T	XP_016861012.1:p.Arg951Ter
XM_017005524.2:c.2584C>T	XP_016861013.1:p.Arg862Ter
XM_017005525.1:c.1951C>T	XP_016861014.1:p.Arg651Ter
NM_005862.3:c.3262C>T MANE Select	NP_005853.2:p.Arg1088Ter