Canonical Allele Identifier: CA1191068921

Gene: CD58

Linked Data

• dbSNP Id: rs1658120151

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116545097_116545100del , CM000663.2:g.116545097_116545100del	GRCh38
NC_000001.10:g.117087719_117087722del , CM000663.1:g.117087719_117087722del	GRCh37
NC_000001.9:g.116889242_116889245del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.71-492_71-489del MANE Select	ENSP00000358501.5:n.71-492_71-489del
ENST00000369487.3:c.71-492_71-489del	ENSP00000358499.3:n.71-492_71-489del
ENST00000369489.9:c.71-492_71-489del	ENSP00000358501.5:n.71-492_71-489del
ENST00000457047.6:c.71-492_71-489del	ENSP00000409080.2:n.71-492_71-489del
ENST00000464088.5:c.71-492_71-489del	ENSP00000432773.1:n.71-492_71-489del
NM_001144822.1:c.71-492_71-489del	NP_001138294.1:n.71-492_71-489del
NM_001779.2:c.71-492_71-489del	NP_001770.1:n.71-492_71-489del
NR_026665.1:n.192-492_192-489del
XR_947739.1:n.210+273_210+276del
XR_947740.1:n.210+273_210+276del
XM_017002869.2:c.71-492_71-489del	XP_016858358.1:n.71-492_71-489del
NM_001779.3:c.71-492_71-489del MANE Select	NP_001770.1:n.71-492_71-489del
NR_026665.2:n.125-492_125-489del
NM_001144822.2:c.71-492_71-489del	NP_001138294.1:n.71-492_71-489del