Canonical Allele Identifier: CA10235932

Gene: SUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38750308A>G , CM000684.2:g.38750308A>G	GRCh38
NC_000022.10:g.39146313A>G , CM000684.1:g.39146313A>G	GRCh37
NC_000022.9:g.37476259A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015374.3:c.437T>C MANE Select	NP_056189.1:p.Val146Ala
ENST00000689035.1:c.437T>C MANE Select	ENSP00000508608.1:p.Val146Ala
NM_001199579.1:c.500T>C	NP_001186508.1:p.Val167Ala
NM_001199579.2:c.500T>C	NP_001186508.1:p.Val167Ala
NM_001199580.1:c.437T>C	NP_001186509.1:p.Val146Ala
NM_001199580.2:c.437T>C	NP_001186509.1:p.Val146Ala
NM_001394427.1:c.437T>C	NP_001381356.1:p.Val146Ala
NM_001394428.1:c.500T>C	NP_001381357.1:p.Val167Ala
NM_001394429.1:c.482T>C	NP_001381358.1:p.Val161Ala
NM_001394430.1:c.482T>C	NP_001381359.1:p.Val161Ala
NM_001394431.1:c.437T>C	NP_001381360.1:p.Val146Ala
NM_001394432.1:c.437T>C	NP_001381361.1:p.Val146Ala
NM_001394433.1:c.437T>C	NP_001381362.1:p.Val146Ala
NM_001394434.1:c.437T>C	NP_001381363.1:p.Val146Ala
NM_001394435.1:c.437T>C	NP_001381364.1:p.Val146Ala
NM_001394436.1:c.437T>C	NP_001381365.1:p.Val146Ala
NM_001394437.1:c.437T>C	NP_001381366.1:p.Val146Ala
NM_001394438.1:c.347T>C	NP_001381367.1:p.Val116Ala
NM_001394439.1:c.299T>C	NP_001381368.1:p.Val100Ala
NM_001394440.1:c.299T>C	NP_001381369.1:p.Val100Ala
NM_001394441.1:c.299T>C	NP_001381370.1:p.Val100Ala
NM_001394442.1:c.437T>C	NP_001381371.1:p.Val146Ala
NM_001394443.1:c.123-1525T>C	NP_001381372.1:n.123-1525T>C
NM_001394444.1:c.437T>C	NP_001381373.1:p.Val146Ala
NM_001394445.1:c.437T>C	NP_001381374.1:p.Val146Ala
NM_015374.2:c.437T>C	NP_056189.1:p.Val146Ala
ENST00000405018.5:c.500T>C	ENSP00000385616.1:p.Val167Ala
ENST00000405510.5:c.437T>C	ENSP00000385740.1:p.Val146Ala
ENST00000406622.5:c.437T>C	ENSP00000383992.1:p.Val146Ala
ENST00000420859.5:c.299T>C	ENSP00000408834.1:p.Val100Ala
ENST00000430185.5:c.7T>C
ENST00000438058.5:c.299T>C	ENSP00000406941.1:p.Val100Ala
ENST00000455125.2:c.437T>C	ENSP00000390154.2:p.Val146Ala
ENST00000456894.5:c.437T>C	ENSP00000415588.2:p.Val146Ala
ENST00000456894.6:c.299T>C	ENSP00000415588.3:p.Val100Ala
ENST00000480307.1:n.383T>C
ENST00000690927.1:c.437T>C	ENSP00000508791.1:p.Val146Ala
XM_011530104.1:c.299T>C	XP_011528406.1:p.Val100Ala
XM_011530104.2:c.299T>C	XP_011528406.1:p.Val100Ala
XM_011530105.1:c.404T>C	XP_011528407.1:p.Val135Ala
XM_011530105.2:c.404T>C	XP_011528407.1:p.Val135Ala
XM_017028748.1:c.437T>C	XP_016884237.1:p.Val146Ala
XM_024452203.1:c.716T>C	XP_024307971.1:p.Val239Ala
XM_024452204.1:c.542T>C	XP_024307972.1:p.Val181Ala
XM_024452205.1:c.437T>C	XP_024307973.1:p.Val146Ala
XM_024452206.1:c.299T>C	XP_024307974.1:p.Val100Ala