Canonical Allele Identifier: CA514781249
Gene: SUN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38738975G>A , CM000684.2:g.38738975G>A GRCh38
NC_000022.10:g.39134980G>A , CM000684.1:g.39134980G>A GRCh37
NC_000022.9:g.37464926G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015374.3:c.1677C>T MANE Select NP_056189.1:p.Ile559=
ENST00000689035.1:c.1677C>T MANE Select ENSP00000508608.1:p.Ile559=
NM_001199579.1:c.1740C>T NP_001186508.1:p.Ile580=
NM_001199579.2:c.1740C>T NP_001186508.1:p.Ile580=
NM_001199580.1:c.1677C>T NP_001186509.1:p.Ile559=
NM_001199580.2:c.1677C>T NP_001186509.1:p.Ile559=
NM_001394427.1:c.1770C>T NP_001381356.1:p.Ile590=
NM_001394428.1:c.1740C>T NP_001381357.1:p.Ile580=
NM_001394429.1:c.1722C>T NP_001381358.1:p.Ile574=
NM_001394430.1:c.1722C>T NP_001381359.1:p.Ile574=
NM_001394431.1:c.1677C>T NP_001381360.1:p.Ile559=
NM_001394432.1:c.1677C>T NP_001381361.1:p.Ile559=
NM_001394433.1:c.1677C>T NP_001381362.1:p.Ile559=
NM_001394434.1:c.1677C>T NP_001381363.1:p.Ile559=
NM_001394435.1:c.1677C>T NP_001381364.1:p.Ile559=
NM_001394436.1:c.1674C>T NP_001381365.1:p.Ile558=
NM_001394437.1:c.1674C>T NP_001381366.1:p.Ile558=
NM_001394438.1:c.1587C>T NP_001381367.1:p.Ile529=
NM_001394439.1:c.1539C>T NP_001381368.1:p.Ile513=
NM_001394440.1:c.1539C>T NP_001381369.1:p.Ile513=
NM_001394441.1:c.1539C>T NP_001381370.1:p.Ile513=
NM_001394442.1:c.1278C>T NP_001381371.1:p.Ile426=
NM_001394443.1:c.1185C>T NP_001381372.1:p.Ile395=
NM_001394444.1:c.1101C>T NP_001381373.1:p.Ile367=
NM_001394445.1:c.1101C>T NP_001381374.1:p.Ile367=
NM_015374.2:c.1677C>T NP_056189.1:p.Ile559=
ENST00000405018.5:c.1740C>T ENSP00000385616.1:p.Ile580=
ENST00000405510.5:c.1677C>T ENSP00000385740.1:p.Ile559=
ENST00000406622.5:c.1677C>T ENSP00000383992.1:p.Ile559=
ENST00000455125.1:c.96C>T ENSP00000390154.1:p.Ile32=
ENST00000455125.2:c.1677C>T ENSP00000390154.2:p.Ile559=
ENST00000456894.6:c.1539C>T ENSP00000415588.3:p.Ile513=
ENST00000470642.1:n.273C>T
ENST00000477262.5:n.865C>T
ENST00000690927.1:c.1443C>T ENSP00000508791.1:p.Ile481=
XM_011530104.1:c.1539C>T XP_011528406.1:p.Ile513=
XM_011530104.2:c.1539C>T XP_011528406.1:p.Ile513=
XM_011530105.1:c.1644C>T XP_011528407.1:p.Ile548=
XM_011530105.2:c.1644C>T XP_011528407.1:p.Ile548=
XM_017028748.1:c.1677C>T XP_016884237.1:p.Ile559=
XM_024452203.1:c.1956C>T XP_024307971.1:p.Ile652=
XM_024452204.1:c.1782C>T XP_024307972.1:p.Ile594=
XM_024452205.1:c.1677C>T XP_024307973.1:p.Ile559=
XM_024452206.1:c.1539C>T XP_024307974.1:p.Ile513=