Canonical Allele Identifier: CA1729411548

Gene: STAG3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100180604G= , CM000669.2:g.100180604G=	GRCh38
NC_000007.13:g.99778227G= , CM000669.1:g.99778227G=	GRCh37
NC_000007.12:g.99616163G=	NCBI36
NG_034114.1:g.7881G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001282717.2:c.48G= MANE Select	NP_001269646.1:p.Leu16=
ENST00000615138.5:c.48G= MANE Select	ENSP00000477973.1:p.Leu16=
NM_001282716.1:c.48G=	NP_001269645.1:p.Leu16=
NM_001282717.1:c.48G=	NP_001269646.1:p.Leu16=
NM_001282718.1:c.48G=	NP_001269647.1:p.Leu16=
NM_001282718.2:c.48G=	NP_001269647.1:p.Leu16=
NM_001375438.1:c.48G=	NP_001362367.1:p.Leu16=
NM_012447.3:c.48G=	NP_036579.2:p.Leu16=
NM_012447.4:c.48G=	NP_036579.2:p.Leu16=
ENST00000317296.9:c.48G=	ENSP00000319318.5:p.Leu16=
ENST00000394018.6:c.48G=	ENSP00000377586.2:p.Leu16=
ENST00000412190.6:c.48G=	ENSP00000395039.2:p.Leu16=
ENST00000416412.5:c.48G=	ENSP00000409283.1:p.Leu16=
ENST00000422690.5:c.48G=	ENSP00000407884.1:p.Leu16=
ENST00000426455.5:c.48G=	ENSP00000400359.1:p.Leu16=
ENST00000439782.1:c.48G=	ENSP00000397067.1:p.Leu16=
ENST00000482546.1:n.181G=
ENST00000496157.5:n.183G=
ENST00000615138.4:c.48G=	ENSP00000477973.1:p.Leu16=
ENST00000620100.4:c.48G=	ENSP00000484098.1:p.Leu16=
ENST00000620100.5:c.48G=	ENSP00000484098.1:p.Leu16=
XM_005250116.1:c.48G=	XP_005250173.1:p.Leu16=
XM_011515742.1:c.48G=	XP_011514044.1:p.Leu16=
XM_011515743.1:c.48G=	XP_011514045.1:p.Leu16=
XM_011515744.1:c.48G=	XP_011514046.1:p.Leu16=
XM_017011683.2:c.48G=	XP_016867172.1:p.Leu16=
XM_017011684.1:c.48G=	XP_016867173.1:p.Leu16=
XM_017011685.1:c.48G=	XP_016867174.1:p.Leu16=
XM_017011686.2:c.48G=	XP_016867175.1:p.Leu16=
XM_017011687.1:c.48G=	XP_016867176.1:p.Leu16=