Canonical Allele Identifier: CA1191068947

Gene: CD58

Linked Data

• dbSNP Id: rs1658123255

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116545162del , CM000663.2:g.116545162del	GRCh38
NC_000001.10:g.117087784del , CM000663.1:g.117087784del	GRCh37
NC_000001.9:g.116889307del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369489.10:c.71-557del MANE Select	ENSP00000358501.5:n.71-557del
ENST00000369487.3:c.71-557del	ENSP00000358499.3:n.71-557del
ENST00000369489.9:c.71-557del	ENSP00000358501.5:n.71-557del
ENST00000457047.6:c.71-557del	ENSP00000409080.2:n.71-557del
ENST00000464088.5:c.71-557del	ENSP00000432773.1:n.71-557del
NM_001144822.1:c.71-557del	NP_001138294.1:n.71-557del
NM_001779.2:c.71-557del	NP_001770.1:n.71-557del
NR_026665.1:n.192-557del
XR_947739.1:n.210+338del
XR_947740.1:n.210+338del
XM_017002869.2:c.71-557del	XP_016858358.1:n.71-557del
NM_001779.3:c.71-557del MANE Select	NP_001770.1:n.71-557del
NR_026665.2:n.125-557del
NM_001144822.2:c.71-557del	NP_001138294.1:n.71-557del