Canonical Allele Identifier: CA411584153
Gene: SUN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38739790C>G , CM000684.2:g.38739790C>G GRCh38
NC_000022.10:g.39135795C>G , CM000684.1:g.39135795C>G GRCh37
NC_000022.9:g.37465741C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015374.3:c.1510G>C MANE Select NP_056189.1:p.Ala504Pro
ENST00000689035.1:c.1510G>C MANE Select ENSP00000508608.1:p.Ala504Pro
NM_001199579.1:c.1573G>C NP_001186508.1:p.Ala525Pro
NM_001199579.2:c.1573G>C NP_001186508.1:p.Ala525Pro
NM_001199580.1:c.1510G>C NP_001186509.1:p.Ala504Pro
NM_001199580.2:c.1510G>C NP_001186509.1:p.Ala504Pro
NM_001394427.1:c.1603G>C NP_001381356.1:p.Ala535Pro
NM_001394428.1:c.1573G>C NP_001381357.1:p.Ala525Pro
NM_001394429.1:c.1555G>C NP_001381358.1:p.Ala519Pro
NM_001394430.1:c.1555G>C NP_001381359.1:p.Ala519Pro
NM_001394431.1:c.1510G>C NP_001381360.1:p.Ala504Pro
NM_001394432.1:c.1510G>C NP_001381361.1:p.Ala504Pro
NM_001394433.1:c.1510G>C NP_001381362.1:p.Ala504Pro
NM_001394434.1:c.1510G>C NP_001381363.1:p.Ala504Pro
NM_001394435.1:c.1510G>C NP_001381364.1:p.Ala504Pro
NM_001394436.1:c.1510G>C NP_001381365.1:p.Ala504Pro
NM_001394437.1:c.1510G>C NP_001381366.1:p.Ala504Pro
NM_001394438.1:c.1420G>C NP_001381367.1:p.Ala474Pro
NM_001394439.1:c.1372G>C NP_001381368.1:p.Ala458Pro
NM_001394440.1:c.1372G>C NP_001381369.1:p.Ala458Pro
NM_001394441.1:c.1372G>C NP_001381370.1:p.Ala458Pro
NM_001394442.1:c.1111G>C NP_001381371.1:p.Ala371Pro
NM_001394443.1:c.1018G>C NP_001381372.1:p.Ala340Pro
NM_001394444.1:c.934G>C NP_001381373.1:p.Ala312Pro
NM_001394445.1:c.934G>C NP_001381374.1:p.Ala312Pro
NM_015374.2:c.1510G>C NP_056189.1:p.Ala504Pro
ENST00000405018.5:c.1573G>C ENSP00000385616.1:p.Ala525Pro
ENST00000405510.5:c.1510G>C ENSP00000385740.1:p.Ala504Pro
ENST00000406622.5:c.1510G>C ENSP00000383992.1:p.Ala504Pro
ENST00000455125.2:c.1510G>C ENSP00000390154.2:p.Ala504Pro
ENST00000456894.6:c.1372G>C ENSP00000415588.3:p.Ala458Pro
ENST00000469086.5:n.1197G>C
ENST00000477262.5:n.698G>C
ENST00000690927.1:c.1276G>C ENSP00000508791.1:p.Ala426Pro
XM_011530104.1:c.1372G>C XP_011528406.1:p.Ala458Pro
XM_011530104.2:c.1372G>C XP_011528406.1:p.Ala458Pro
XM_011530105.1:c.1477G>C XP_011528407.1:p.Ala493Pro
XM_011530105.2:c.1477G>C XP_011528407.1:p.Ala493Pro
XM_017028748.1:c.1510G>C XP_016884237.1:p.Ala504Pro
XM_024452203.1:c.1789G>C XP_024307971.1:p.Ala597Pro
XM_024452204.1:c.1615G>C XP_024307972.1:p.Ala539Pro
XM_024452205.1:c.1510G>C XP_024307973.1:p.Ala504Pro
XM_024452206.1:c.1372G>C XP_024307974.1:p.Ala458Pro