Canonical Allele Identifier: CA2696928097

Gene: CD58

Linked Data

• dbSNP Id: rs2101191165

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116545103C>T , CM000663.2:g.116545103C>T	GRCh38
NC_000001.10:g.117087725C>T , CM000663.1:g.117087725C>T	GRCh37
NC_000001.9:g.116889248C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.71-499G>A MANE Select	ENSP00000358501.5:n.71-499G>A
ENST00000369487.3:c.71-499G>A	ENSP00000358499.3:n.71-499G>A
ENST00000369489.9:c.71-499G>A	ENSP00000358501.5:n.71-499G>A
ENST00000457047.6:c.71-499G>A	ENSP00000409080.2:n.71-499G>A
ENST00000464088.5:c.71-499G>A	ENSP00000432773.1:n.71-499G>A
NM_001144822.1:c.71-499G>A	NP_001138294.1:n.71-499G>A
NM_001779.2:c.71-499G>A	NP_001770.1:n.71-499G>A
NR_026665.1:n.192-499G>A
XR_947739.1:n.210+279C>T
XR_947740.1:n.210+279C>T
XM_017002869.2:c.71-499G>A	XP_016858358.1:n.71-499G>A
NM_001779.3:c.71-499G>A MANE Select	NP_001770.1:n.71-499G>A
NR_026665.2:n.125-499G>A
NM_001144822.2:c.71-499G>A	NP_001138294.1:n.71-499G>A