Canonical Allele Identifier: CA10235411

Gene: SUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38738703C>T , CM000684.2:g.38738703C>T	GRCh38
NC_000022.10:g.39134708C>T , CM000684.1:g.39134708C>T	GRCh37
NC_000022.9:g.37464654C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455125.2:c.1831G>A	ENSP00000390154.2:p.Ala611Thr
ENST00000456894.6:c.1693G>A	ENSP00000415588.3:p.Ala565Thr
ENST00000689035.1:c.1831G>A MANE Select	ENSP00000508608.1:p.Ala611Thr
ENST00000690927.1:c.1597G>A	ENSP00000508791.1:p.Ala533Thr
ENST00000405018.5:c.1894G>A	ENSP00000385616.1:p.Ala632Thr
ENST00000405510.5:c.1831G>A	ENSP00000385740.1:p.Ala611Thr
ENST00000406622.5:c.1831G>A	ENSP00000383992.1:p.Ala611Thr
ENST00000455125.1:c.250G>A	ENSP00000390154.1:p.Ala84Thr
ENST00000470642.1:n.427G>A
NM_001199579.1:c.1894G>A	NP_001186508.1:p.Ala632Thr
NM_001199580.1:c.1831G>A	NP_001186509.1:p.Ala611Thr
NM_015374.2:c.1831G>A	NP_056189.1:p.Ala611Thr
XM_011530104.1:c.1693G>A	XP_011528406.1:p.Ala565Thr
XM_011530105.1:c.1798G>A	XP_011528407.1:p.Ala600Thr
XM_011530104.2:c.1693G>A	XP_011528406.1:p.Ala565Thr
XM_011530105.2:c.1798G>A	XP_011528407.1:p.Ala600Thr
XM_017028748.1:c.1831G>A	XP_016884237.1:p.Ala611Thr
XM_024452203.1:c.2110G>A	XP_024307971.1:p.Ala704Thr
XM_024452204.1:c.1936G>A	XP_024307972.1:p.Ala646Thr
XM_024452205.1:c.1831G>A	XP_024307973.1:p.Ala611Thr
XM_024452206.1:c.1693G>A	XP_024307974.1:p.Ala565Thr
NM_001199579.2:c.1894G>A	NP_001186508.1:p.Ala632Thr
NM_001199580.2:c.1831G>A	NP_001186509.1:p.Ala611Thr
NM_015374.3:c.1831G>A MANE Select	NP_056189.1:p.Ala611Thr
NM_001394427.1:c.1924G>A	NP_001381356.1:p.Ala642Thr
NM_001394428.1:c.1894G>A	NP_001381357.1:p.Ala632Thr
NM_001394429.1:c.1876G>A	NP_001381358.1:p.Ala626Thr
NM_001394430.1:c.1876G>A	NP_001381359.1:p.Ala626Thr
NM_001394431.1:c.1831G>A	NP_001381360.1:p.Ala611Thr
NM_001394432.1:c.1831G>A	NP_001381361.1:p.Ala611Thr
NM_001394433.1:c.1831G>A	NP_001381362.1:p.Ala611Thr
NM_001394434.1:c.1831G>A	NP_001381363.1:p.Ala611Thr
NM_001394435.1:c.1831G>A	NP_001381364.1:p.Ala611Thr
NM_001394436.1:c.1828G>A	NP_001381365.1:p.Ala610Thr
NM_001394437.1:c.1828G>A	NP_001381366.1:p.Ala610Thr
NM_001394438.1:c.1741G>A	NP_001381367.1:p.Ala581Thr
NM_001394439.1:c.1693G>A	NP_001381368.1:p.Ala565Thr
NM_001394440.1:c.1693G>A	NP_001381369.1:p.Ala565Thr
NM_001394441.1:c.1693G>A	NP_001381370.1:p.Ala565Thr
NM_001394442.1:c.1432G>A	NP_001381371.1:p.Ala478Thr
NM_001394443.1:c.1339G>A	NP_001381372.1:p.Ala447Thr
NM_001394444.1:c.1255G>A	NP_001381373.1:p.Ala419Thr
NM_001394445.1:c.1255G>A	NP_001381374.1:p.Ala419Thr