Canonical Allele Identifier: CA84286657

Gene: STAG1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136683218G>A , CM000665.2:g.136683218G>A	GRCh38
NC_000003.11:g.136402060G>A , CM000665.1:g.136402060G>A	GRCh37
NC_000003.10:g.137884750G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383202.7:c.-83-52237C>T MANE Select	ENSP00000372689.2:n.-83-52237C>T
ENST00000236698.9:c.-83-52237C>T	ENSP00000236698.5:n.-83-52237C>T
ENST00000383202.6:c.-83-52237C>T	ENSP00000372689.2:n.-83-52237C>T
ENST00000434713.6:c.-761-52237C>T	ENSP00000404396.2:n.-761-52237C>T
ENST00000480733.1:c.-83-52237C>T	ENSP00000420789.1:n.-83-52237C>T
ENST00000483235.5:c.-83-52237C>T	ENSP00000419093.1:n.-83-52237C>T
ENST00000487065.5:c.-83-52237C>T	ENSP00000418472.1:n.-83-52237C>T
ENST00000629124.2:c.-83-52237C>T	ENSP00000486745.1:n.-83-52237C>T
NM_005862.2:c.-83-52237C>T	NP_005853.2:n.-83-52237C>T
XM_011512329.1:c.-724-52237C>T	XP_011510631.1:n.-724-52237C>T
XM_011512331.1:c.-619-52237C>T	XP_011510633.1:n.-619-52237C>T
XM_011512329.2:c.-724-52237C>T	XP_011510631.1:n.-724-52237C>T
XM_011512331.2:c.-619-52237C>T	XP_011510633.1:n.-619-52237C>T
XM_017005523.1:c.-397-52237C>T	XP_016861012.1:n.-397-52237C>T
XM_017005524.2:c.-826-52237C>T	XP_016861013.1:n.-826-52237C>T
XR_001739978.1:n.196-52237C>T
NM_005862.3:c.-83-52237C>T MANE Select	NP_005853.2:n.-83-52237C>T