Canonical Allele Identifier: CA2597076674

Gene: SUN3

Linked Data

• gnomAD v3: 7-47991842-CTAACAGTCA-C
• gnomAD v4: 7-47991842-CTAACAGTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.47991844_47991852del , CM000669.2:g.47991844_47991852del	GRCh38
NC_000007.13:g.48031441_48031449del , CM000669.1:g.48031441_48031449del	GRCh37
NC_000007.12:g.47997966_47997974del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297325.9:c.861+2464_861+2472del MANE Select	ENSP00000297325.4:n.861+2464_861+2472del
ENST00000297325.8:c.861+2464_861+2472del	ENSP00000297325.4:n.861+2464_861+2472del
ENST00000395572.6:c.861+2464_861+2472del	ENSP00000378939.2:n.861+2464_861+2472del
ENST00000412142.5:c.825+2464_825+2472del	ENSP00000410204.2:n.825+2464_825+2472del
ENST00000412371.5:c.327+2464_327+2472del	ENSP00000406887.1:n.327+2464_327+2472del
ENST00000438771.5:c.562-806_562-798del	ENSP00000409077.1:n.562-806_562-798del
ENST00000449896.2:c.*689+2464_*689+2472del	ENSP00000395392.2:n.*689+2464_*689+2472del
ENST00000453071.5:c.632+2464_632+2472del
ENST00000453192.3:c.573+2452_573+2460del	ENSP00000387525.3:n.573+2452_573+2460del
ENST00000473723.5:n.339-806_339-798del
NM_001030019.1:c.861+2464_861+2472del	NP_001025190.1:n.861+2464_861+2472del
NM_001284350.1:c.825+2464_825+2472del	NP_001271279.1:n.825+2464_825+2472del
NM_152782.3:c.861+2464_861+2472del	NP_689995.3:n.861+2464_861+2472del
XM_011515252.1:c.883-806_883-798del	XP_011513554.1:n.883-806_883-798del
XM_011515253.1:c.583-806_583-798del	XP_011513555.1:n.583-806_583-798del
XM_017011930.1:c.861+2464_861+2472del	XP_016867419.1:n.861+2464_861+2472del
XR_002956417.1:n.1148+1040_1148+1048del
NM_001030019.2:c.861+2464_861+2472del MANE Select	NP_001025190.1:n.861+2464_861+2472del
NM_001284350.2:c.825+2464_825+2472del	NP_001271279.1:n.825+2464_825+2472del
NM_152782.4:c.861+2464_861+2472del	NP_689995.3:n.861+2464_861+2472del