Canonical Allele Identifier: CA354652554

Gene: STAG1

Linked Data

• MyVariant Identifiers: chr3:g.136062724C>A (hg19) ; chr3:g.136343882C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136343882C>A , CM000665.2:g.136343882C>A	GRCh38
NC_000003.11:g.136062724C>A , CM000665.1:g.136062724C>A	GRCh37
NC_000003.10:g.137545414C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383202.7:c.3396G>T MANE Select	ENSP00000372689.2:p.Gln1132His
ENST00000236698.9:c.3396G>T	ENSP00000236698.5:p.Gln1132His
ENST00000383202.6:c.3396G>T	ENSP00000372689.2:p.Gln1132His
ENST00000434713.6:c.2616G>T	ENSP00000404396.2:p.Gln872His
ENST00000483235.5:c.*3386G>T	ENSP00000419093.1:n.*3386G>T
ENST00000629124.2:c.*3035G>T	ENSP00000486745.1:n.*3035G>T
NM_005862.2:c.3396G>T	NP_005853.2:p.Gln1132His
XM_011512329.1:c.2985G>T	XP_011510631.1:p.Gln995His
XM_011512330.1:c.2985G>T	XP_011510632.1:p.Gln995His
XM_011512331.1:c.2985G>T	XP_011510633.1:p.Gln995His
XM_011512332.1:c.2718G>T	XP_011510634.1:p.Gln906His
XM_011512333.1:c.2985G>T	XP_011510635.1:p.Gln995His
XM_011512329.2:c.2985G>T	XP_011510631.1:p.Gln995His
XM_011512331.2:c.2985G>T	XP_011510633.1:p.Gln995His
XM_017005523.1:c.2985G>T	XP_016861012.1:p.Gln995His
XM_017005524.2:c.2718G>T	XP_016861013.1:p.Gln906His
XM_017005525.1:c.2085G>T	XP_016861014.1:p.Gln695His
NM_005862.3:c.3396G>T MANE Select	NP_005853.2:p.Gln1132His