Canonical Allele Identifier: CA351877929

Gene: SGO1 SGO1-AS1

Linked Data

• MyVariant Identifiers: chr3:g.20225434T>A (hg19) ; chr3:g.20183942T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.20183942T>A , CM000665.2:g.20183942T>A	GRCh38
NC_000003.11:g.20225434T>A , CM000665.1:g.20225434T>A	GRCh37
NC_000003.10:g.20200438T>A	NCBI36
NG_042062.1:g.7290A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412997.6:c.86A>T (SGO1) MANE Select	ENSP00000410458.1:p.Asn29Ile
ENST00000263753.8:c.86A>T (SGO1)	ENSP00000263753.4:p.Asn29Ile
ENST00000306698.6:c.86A>T (SGO1)	ENSP00000306581.2:p.Asn29Ile
ENST00000412997.5:c.86A>T (SGO1)	ENSP00000410458.1:p.Asn29Ile
ENST00000417364.1:c.86A>T (SGO1)	ENSP00000394613.1:p.Asn29Ile
ENST00000419233.6:c.86A>T (SGO1)	ENSP00000394625.2:p.Asn29Ile
ENST00000421451.5:c.86A>T (SGO1)	ENSP00000414129.1:p.Asn29Ile
ENST00000425061.5:c.86A>T (SGO1)	ENSP00000414960.1:p.Asn29Ile
ENST00000437051.5:c.86A>T (SGO1)	ENSP00000389034.1:p.Asn29Ile
ENST00000442720.5:c.86A>T (SGO1)	ENSP00000394957.1:p.Asn29Ile
ENST00000443724.5:c.86A>T (SGO1)	ENSP00000413070.1:p.Asn29Ile
ENST00000452020.5:c.86A>T (SGO1)	ENSP00000411200.1:p.Asn29Ile
ENST00000456624.1:c.86A>T (SGO1)	ENSP00000397672.1:p.Asn29Ile
NM_001012409.2:c.86A>T (SGO1)	NP_001012409.1:p.Asn29Ile
NM_001012409.3:c.86A>T (SGO1)	NP_001012409.1:p.Asn29Ile
NM_001012410.3:c.86A>T (SGO1)	NP_001012410.1:p.Asn29Ile
NM_001012410.4:c.86A>T (SGO1)	NP_001012410.1:p.Asn29Ile
NM_001012411.2:c.86A>T (SGO1)	NP_001012411.1:p.Asn29Ile
NM_001012411.3:c.86A>T (SGO1)	NP_001012411.1:p.Asn29Ile
NM_001012412.3:c.86A>T (SGO1)	NP_001012412.1:p.Asn29Ile
NM_001012412.4:c.86A>T (SGO1)	NP_001012412.1:p.Asn29Ile
NM_001012413.2:c.86A>T (SGO1)	NP_001012413.1:p.Asn29Ile
NM_001012413.3:c.86A>T (SGO1)	NP_001012413.1:p.Asn29Ile
NM_001199251.1:c.86A>T (SGO1)	NP_001186180.1:p.Asn29Ile
NM_001199251.2:c.86A>T (SGO1)	NP_001186180.1:p.Asn29Ile
NM_001199252.1:c.86A>T (SGO1)	NP_001186181.1:p.Asn29Ile
NM_001199252.2:c.86A>T (SGO1)	NP_001186181.1:p.Asn29Ile
NM_001199253.1:c.86A>T (SGO1)	NP_001186182.1:p.Asn29Ile
NM_001199253.2:c.86A>T (SGO1)	NP_001186182.1:p.Asn29Ile
NM_001199254.1:c.86A>T (SGO1)	NP_001186183.1:p.Asn29Ile
NM_001199254.2:c.86A>T (SGO1)	NP_001186183.1:p.Asn29Ile
NM_001199255.1:c.86A>T (SGO1)	NP_001186184.1:p.Asn29Ile
NM_001199255.2:c.86A>T (SGO1)	NP_001186184.1:p.Asn29Ile
NM_001199256.1:c.86A>T (SGO1)	NP_001186185.1:p.Asn29Ile
NM_001199256.2:c.86A>T (SGO1)	NP_001186185.1:p.Asn29Ile
NM_001199257.1:c.86A>T (SGO1)	NP_001186186.1:p.Asn29Ile
NM_001199257.2:c.86A>T (SGO1)	NP_001186186.1:p.Asn29Ile
NM_138484.3:c.86A>T (SGO1)	NP_612493.1:p.Asn29Ile
NM_138484.4:c.86A>T (SGO1)	NP_612493.1:p.Asn29Ile
NR_131179.1:n.268A>T (SGO1)
NR_131180.1:n.268A>T (SGO1)
NR_132785.1:n.359-2033T>A (SGO1-AS1)
XM_011533373.1:c.86A>T (SGO1)	XP_011531675.1:p.Asn29Ile
XM_011533374.1:c.86A>T (SGO1)	XP_011531676.1:p.Asn29Ile
XM_011533375.1:c.86A>T (SGO1)	XP_011531677.1:p.Asn29Ile
XM_011533376.1:c.86A>T (SGO1)	XP_011531678.1:p.Asn29Ile
XM_011533377.1:c.86A>T (SGO1)	XP_011531679.1:p.Asn29Ile
XM_011533373.2:c.86A>T (SGO1)	XP_011531675.1:p.Asn29Ile
XM_011533375.2:c.86A>T (SGO1)	XP_011531677.1:p.Asn29Ile
XM_011533376.2:c.86A>T (SGO1)	XP_011531678.1:p.Asn29Ile
XM_011533377.2:c.86A>T (SGO1)	XP_011531679.1:p.Asn29Ile
NM_001199251.3:c.86A>T (SGO1) MANE Select	NP_001186180.1:p.Asn29Ile
NM_001012410.5:c.86A>T (SGO1)	NP_001012410.1:p.Asn29Ile
NM_001012412.5:c.86A>T (SGO1)	NP_001012412.1:p.Asn29Ile
NM_001199252.3:c.86A>T (SGO1)	NP_001186181.1:p.Asn29Ile
NM_001199254.3:c.86A>T (SGO1)	NP_001186183.1:p.Asn29Ile
NM_001199256.3:c.86A>T (SGO1)	NP_001186185.1:p.Asn29Ile
NM_001199257.3:c.86A>T (SGO1)	NP_001186186.1:p.Asn29Ile
NM_138484.5:c.86A>T (SGO1)	NP_612493.1:p.Asn29Ile
NM_001012409.4:c.86A>T (SGO1)	NP_001012409.1:p.Asn29Ile
NM_001012411.4:c.86A>T (SGO1)	NP_001012411.1:p.Asn29Ile
NM_001012413.4:c.86A>T (SGO1)	NP_001012413.1:p.Asn29Ile
NM_001199253.3:c.86A>T (SGO1)	NP_001186182.1:p.Asn29Ile
NM_001199255.3:c.86A>T (SGO1)	NP_001186184.1:p.Asn29Ile
NR_131179.2:n.241A>T (SGO1)
NR_131180.2:n.241A>T (SGO1)