Canonical Allele Identifier: CA10235484

Gene: SUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38739332G>C , CM000684.2:g.38739332G>C	GRCh38
NC_000022.10:g.39135337G>C , CM000684.1:g.39135337G>C	GRCh37
NC_000022.9:g.37465283G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455125.2:c.1663+10C>G	ENSP00000390154.2:n.1663+10C>G
ENST00000456894.6:c.1525+10C>G	ENSP00000415588.3:n.1525+10C>G
ENST00000689035.1:c.1663+10C>G MANE Select	ENSP00000508608.1:n.1663+10C>G
ENST00000690927.1:c.1429+10C>G	ENSP00000508791.1:n.1429+10C>G
ENST00000405018.5:c.1726+10C>G	ENSP00000385616.1:n.1726+10C>G
ENST00000405510.5:c.1663+10C>G	ENSP00000385740.1:n.1663+10C>G
ENST00000406622.5:c.1663+10C>G	ENSP00000383992.1:n.1663+10C>G
ENST00000455125.1:c.82+10C>G	ENSP00000390154.1:n.82+10C>G
ENST00000477262.5:n.851+10C>G
NM_001199579.1:c.1726+10C>G	NP_001186508.1:n.1726+10C>G
NM_001199580.1:c.1663+10C>G	NP_001186509.1:n.1663+10C>G
NM_015374.2:c.1663+10C>G	NP_056189.1:n.1663+10C>G
XM_011530104.1:c.1525+10C>G	XP_011528406.1:n.1525+10C>G
XM_011530105.1:c.1630+10C>G	XP_011528407.1:n.1630+10C>G
XM_011530104.2:c.1525+10C>G	XP_011528406.1:n.1525+10C>G
XM_011530105.2:c.1630+10C>G	XP_011528407.1:n.1630+10C>G
XM_017028748.1:c.1663+10C>G	XP_016884237.1:n.1663+10C>G
XM_024452203.1:c.1942+10C>G	XP_024307971.1:n.1942+10C>G
XM_024452204.1:c.1768+10C>G	XP_024307972.1:n.1768+10C>G
XM_024452205.1:c.1663+10C>G	XP_024307973.1:n.1663+10C>G
XM_024452206.1:c.1525+10C>G	XP_024307974.1:n.1525+10C>G
NM_001199579.2:c.1726+10C>G	NP_001186508.1:n.1726+10C>G
NM_001199580.2:c.1663+10C>G	NP_001186509.1:n.1663+10C>G
NM_015374.3:c.1663+10C>G MANE Select	NP_056189.1:n.1663+10C>G
NM_001394427.1:c.1756+10C>G	NP_001381356.1:n.1756+10C>G
NM_001394428.1:c.1726+10C>G	NP_001381357.1:n.1726+10C>G
NM_001394429.1:c.1708+10C>G	NP_001381358.1:n.1708+10C>G
NM_001394430.1:c.1708+10C>G	NP_001381359.1:n.1708+10C>G
NM_001394431.1:c.1663+10C>G	NP_001381360.1:n.1663+10C>G
NM_001394432.1:c.1663+10C>G	NP_001381361.1:n.1663+10C>G
NM_001394433.1:c.1663+10C>G	NP_001381362.1:n.1663+10C>G
NM_001394434.1:c.1663+10C>G	NP_001381363.1:n.1663+10C>G
NM_001394435.1:c.1663+10C>G	NP_001381364.1:n.1663+10C>G
NM_001394436.1:c.1660+10C>G	NP_001381365.1:n.1660+10C>G
NM_001394437.1:c.1660+10C>G	NP_001381366.1:n.1660+10C>G
NM_001394438.1:c.1573+10C>G	NP_001381367.1:n.1573+10C>G
NM_001394439.1:c.1525+10C>G	NP_001381368.1:n.1525+10C>G
NM_001394440.1:c.1525+10C>G	NP_001381369.1:n.1525+10C>G
NM_001394441.1:c.1525+10C>G	NP_001381370.1:n.1525+10C>G
NM_001394442.1:c.1264+10C>G	NP_001381371.1:n.1264+10C>G
NM_001394443.1:c.1171+10C>G	NP_001381372.1:n.1171+10C>G
NM_001394444.1:c.1087+10C>G	NP_001381373.1:n.1087+10C>G
NM_001394445.1:c.1087+10C>G	NP_001381374.1:n.1087+10C>G