Canonical Allele Identifier: CA368487817

Gene: STAG3 CASTOR3P

Linked Data

• MyVariant Identifiers: chr7:g.99786496T>A (hg19) ; chr7:g.100188873T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100188873T>A , CM000669.2:g.100188873T>A	GRCh38
NC_000007.13:g.99786496T>A , CM000669.1:g.99786496T>A	GRCh37
NC_000007.12:g.99624432T>A	NCBI36
NG_034114.1:g.16150T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000412190.6:c.337-572T>A (STAG3)	ENSP00000395039.2:n.337-572T>A
ENST00000615138.5:c.572T>A (STAG3) MANE Select	ENSP00000477973.1:p.Phe191Tyr
ENST00000620100.5:c.398T>A (STAG3)	ENSP00000484098.1:p.Phe133Tyr
ENST00000317296.9:c.572T>A (STAG3)	ENSP00000319318.5:p.Phe191Tyr
ENST00000394018.6:c.398T>A (STAG3)	ENSP00000377586.2:p.Phe133Tyr
ENST00000426455.5:c.572T>A (STAG3)	ENSP00000400359.1:p.Phe191Tyr
ENST00000439782.1:c.398T>A (STAG3)	ENSP00000397067.1:p.Phe133Tyr
ENST00000459699.1:n.384-572T>A (STAG3)
ENST00000496157.5:n.989T>A (STAG3)
ENST00000615138.4:c.572T>A (STAG3)	ENSP00000477973.1:p.Phe191Tyr
ENST00000620100.4:c.398T>A (STAG3)	ENSP00000484098.1:p.Phe133Tyr
NM_001282716.1:c.572T>A (STAG3)	NP_001269645.1:p.Phe191Tyr
NM_001282717.1:c.572T>A (STAG3)	NP_001269646.1:p.Phe191Tyr
NM_001282718.1:c.398T>A (STAG3)	NP_001269647.1:p.Phe133Tyr
NM_012447.3:c.572T>A (STAG3)	NP_036579.2:p.Phe191Tyr
XM_005250116.1:c.572T>A (STAG3)	XP_005250173.1:p.Phe191Tyr
XM_011515742.1:c.572T>A (STAG3)	XP_011514044.1:p.Phe191Tyr
XM_011515743.1:c.572T>A (STAG3)	XP_011514045.1:p.Phe191Tyr
XM_011515744.1:c.434-572T>A (STAG3)	XP_011514046.1:n.434-572T>A
XM_011515745.1:c.-53+6034T>A (STAG3)	XP_011514047.1:n.-53+6034T>A
XM_017011683.2:c.572T>A (STAG3)	XP_016867172.1:p.Phe191Tyr
XM_017011684.1:c.572T>A (STAG3)	XP_016867173.1:p.Phe191Tyr
XM_017011685.1:c.572T>A (STAG3)	XP_016867174.1:p.Phe191Tyr
XM_017011686.2:c.572T>A (STAG3)	XP_016867175.1:p.Phe191Tyr
XM_017011687.1:c.398T>A (STAG3)	XP_016867176.1:p.Phe133Tyr
XM_017012156.1:c.536-484A>T (CASTOR3P)	XP_016867645.1:n.536-484A>T
NM_001282717.2:c.572T>A (STAG3) MANE Select	NP_001269646.1:p.Phe191Tyr
NM_001282718.2:c.398T>A (STAG3)	NP_001269647.1:p.Phe133Tyr
NM_001375438.1:c.572T>A (STAG3)	NP_001362367.1:p.Phe191Tyr
NM_012447.4:c.572T>A (STAG3)	NP_036579.2:p.Phe191Tyr