Canonical Allele Identifier: CA1705426362

Gene: SUN3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.47991934A= , CM000669.2:g.47991934A=	GRCh38
NC_000007.13:g.48031531A= , CM000669.1:g.48031531A=	GRCh37
NC_000007.12:g.47998056A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297325.9:c.861+2381T= MANE Select	ENSP00000297325.4:n.861+2381T=
ENST00000297325.8:c.861+2381T=	ENSP00000297325.4:n.861+2381T=
ENST00000395572.6:c.861+2381T=	ENSP00000378939.2:n.861+2381T=
ENST00000412142.5:c.825+2381T=	ENSP00000410204.2:n.825+2381T=
ENST00000412371.5:c.327+2381T=	ENSP00000406887.1:n.327+2381T=
ENST00000438771.5:c.562-889T=	ENSP00000409077.1:n.562-889T=
ENST00000449896.2:c.*689+2381T=	ENSP00000395392.2:n.*689+2381T=
ENST00000453071.5:c.632+2381T=
ENST00000453192.3:c.573+2369T=	ENSP00000387525.3:n.573+2369T=
ENST00000473723.5:n.339-889T=
NM_001030019.1:c.861+2381T=	NP_001025190.1:n.861+2381T=
NM_001284350.1:c.825+2381T=	NP_001271279.1:n.825+2381T=
NM_152782.3:c.861+2381T=	NP_689995.3:n.861+2381T=
XM_011515252.1:c.883-889T=	XP_011513554.1:n.883-889T=
XM_011515253.1:c.583-889T=	XP_011513555.1:n.583-889T=
XM_017011930.1:c.861+2381T=	XP_016867419.1:n.861+2381T=
XR_002956417.1:n.1148+957T=
NM_001030019.2:c.861+2381T= MANE Select	NP_001025190.1:n.861+2381T=
NM_001284350.2:c.825+2381T=	NP_001271279.1:n.825+2381T=
NM_152782.4:c.861+2381T=	NP_689995.3:n.861+2381T=