Canonical Allele Identifier: CA354653586

Gene: STAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136542172G>A , CM000665.2:g.136542172G>A	GRCh38
NC_000003.11:g.136261014G>A , CM000665.1:g.136261014G>A	GRCh37
NC_000003.10:g.137743704G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005862.3:c.418C>T MANE Select	NP_005853.2:p.Arg140Ter
ENST00000383202.7:c.418C>T MANE Select	ENSP00000372689.2:p.Arg140Ter
NM_005862.2:c.418C>T	NP_005853.2:p.Arg140Ter
ENST00000236698.9:c.418C>T	ENSP00000236698.5:p.Arg140Ter
ENST00000383202.6:c.418C>T	ENSP00000372689.2:p.Arg140Ter
ENST00000434713.6:c.-261C>T	ENSP00000404396.2:n.-261C>T
ENST00000462818.1:n.286C>T
ENST00000480733.1:c.418C>T	ENSP00000420789.1:p.Arg140Ter
ENST00000483235.5:c.*342C>T	ENSP00000419093.1:n.*342C>T
ENST00000487065.5:c.*57C>T	ENSP00000418472.1:n.*57C>T
ENST00000629124.2:c.*57C>T	ENSP00000486745.1:n.*57C>T
XM_011512329.1:c.7C>T	XP_011510631.1:p.Arg3Ter
XM_011512329.2:c.7C>T	XP_011510631.1:p.Arg3Ter
XM_011512330.1:c.7C>T	XP_011510632.1:p.Arg3Ter
XM_011512331.1:c.7C>T	XP_011510633.1:p.Arg3Ter
XM_011512331.2:c.7C>T	XP_011510633.1:p.Arg3Ter
XM_011512333.1:c.7C>T	XP_011510635.1:p.Arg3Ter
XM_017005523.1:c.7C>T	XP_016861012.1:p.Arg3Ter
XM_017005524.2:c.-429C>T	XP_016861013.1:n.-429C>T
XR_001739978.1:n.696C>T