Canonical Allele Identifier: CA368481653
Gene: STAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.99778227G>C (hg19) chr7:g.100180604G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000412190.6:c.48G>C ENSP00000395039.2:p.Leu16Phe
ENST00000615138.5:c.48G>C MANE Select ENSP00000477973.1:p.Leu16Phe
ENST00000620100.5:c.48G>C ENSP00000484098.1:p.Leu16Phe
ENST00000317296.9:c.48G>C ENSP00000319318.5:p.Leu16Phe
ENST00000394018.6:c.48G>C ENSP00000377586.2:p.Leu16Phe
ENST00000416412.5:c.48G>C ENSP00000409283.1:p.Leu16Phe
ENST00000422690.5:c.48G>C ENSP00000407884.1:p.Leu16Phe
ENST00000426455.5:c.48G>C ENSP00000400359.1:p.Leu16Phe
ENST00000439782.1:c.48G>C ENSP00000397067.1:p.Leu16Phe
ENST00000482546.1:n.181G>C
ENST00000496157.5:n.183G>C
ENST00000615138.4:c.48G>C ENSP00000477973.1:p.Leu16Phe
ENST00000620100.4:c.48G>C ENSP00000484098.1:p.Leu16Phe
NM_001282716.1:c.48G>C NP_001269645.1:p.Leu16Phe
NM_001282717.1:c.48G>C NP_001269646.1:p.Leu16Phe
NM_001282718.1:c.48G>C NP_001269647.1:p.Leu16Phe
NM_012447.3:c.48G>C NP_036579.2:p.Leu16Phe
XM_005250116.1:c.48G>C XP_005250173.1:p.Leu16Phe
XM_011515742.1:c.48G>C XP_011514044.1:p.Leu16Phe
XM_011515743.1:c.48G>C XP_011514045.1:p.Leu16Phe
XM_011515744.1:c.48G>C XP_011514046.1:p.Leu16Phe
XM_017011683.2:c.48G>C XP_016867172.1:p.Leu16Phe
XM_017011684.1:c.48G>C XP_016867173.1:p.Leu16Phe
XM_017011685.1:c.48G>C XP_016867174.1:p.Leu16Phe
XM_017011686.2:c.48G>C XP_016867175.1:p.Leu16Phe
XM_017011687.1:c.48G>C XP_016867176.1:p.Leu16Phe
NM_001282717.2:c.48G>C MANE Select NP_001269646.1:p.Leu16Phe
NM_001282718.2:c.48G>C NP_001269647.1:p.Leu16Phe
NM_001375438.1:c.48G>C NP_001362367.1:p.Leu16Phe
NM_012447.4:c.48G>C NP_036579.2:p.Leu16Phe
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