Canonical Allele Identifier: CA368484769
Gene: STAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 451295
ClinVar RCV Id: RCV000521752
dbSNP Id: rs1296715259

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100186198A>C , CM000669.2:g.100186198A>C GRCh38
NC_000007.13:g.99783821A>C , CM000669.1:g.99783821A>C GRCh37
NC_000007.12:g.99621757A>C NCBI36
NG_034114.1:g.13475A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000412190.6:c.337-3247A>C ENSP00000395039.2:n.337-3247A>C
ENST00000615138.5:c.337-2A>C MANE Select ENSP00000477973.1:n.337-2A>C
ENST00000620100.5:c.337-2614A>C ENSP00000484098.1:n.337-2614A>C
ENST00000317296.9:c.337-2A>C ENSP00000319318.5:n.337-2A>C
ENST00000394018.6:c.337-2614A>C ENSP00000377586.2:n.337-2614A>C
ENST00000416412.5:c.337-2A>C ENSP00000409283.1:n.337-2A>C
ENST00000426455.5:c.337-2A>C ENSP00000400359.1:n.337-2A>C
ENST00000439782.1:c.337-2614A>C ENSP00000397067.1:n.337-2614A>C
ENST00000459699.1:n.384-3247A>C
ENST00000496157.5:n.472-2A>C
ENST00000615138.4:c.337-2A>C ENSP00000477973.1:n.337-2A>C
ENST00000620100.4:c.337-2614A>C ENSP00000484098.1:n.337-2614A>C
NM_001282716.1:c.337-2A>C NP_001269645.1:n.337-2A>C
NM_001282717.1:c.337-2A>C NP_001269646.1:n.337-2A>C
NM_001282718.1:c.337-2614A>C NP_001269647.1:n.337-2614A>C
NM_012447.3:c.337-2A>C NP_036579.2:n.337-2A>C
XM_005250116.1:c.337-2A>C XP_005250173.1:n.337-2A>C
XM_011515742.1:c.337-2A>C XP_011514044.1:n.337-2A>C
XM_011515743.1:c.337-2A>C XP_011514045.1:n.337-2A>C
XM_011515744.1:c.337-2A>C XP_011514046.1:n.337-2A>C
XM_011515745.1:c.-53+3359A>C XP_011514047.1:n.-53+3359A>C
XM_017011683.2:c.337-2A>C XP_016867172.1:n.337-2A>C
XM_017011684.1:c.337-2A>C XP_016867173.1:n.337-2A>C
XM_017011685.1:c.337-2A>C XP_016867174.1:n.337-2A>C
XM_017011686.2:c.337-2A>C XP_016867175.1:n.337-2A>C
XM_017011687.1:c.337-2614A>C XP_016867176.1:n.337-2614A>C
NM_001282717.2:c.337-2A>C MANE Select NP_001269646.1:n.337-2A>C
NM_001282718.2:c.337-2614A>C NP_001269647.1:n.337-2614A>C
NM_001375438.1:c.337-2A>C NP_001362367.1:n.337-2A>C
NM_012447.4:c.337-2A>C NP_036579.2:n.337-2A>C