Canonical Allele Identifier: CA1191068908

Gene: CD58

Linked Data

• dbSNP Id: rs1658119071

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116545055_116545057del , CM000663.2:g.116545055_116545057del	GRCh38
NC_000001.10:g.117087677_117087679del , CM000663.1:g.117087677_117087679del	GRCh37
NC_000001.9:g.116889200_116889202del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.71-453_71-451del MANE Select	ENSP00000358501.5:n.71-453_71-451del
ENST00000369487.3:c.71-453_71-451del	ENSP00000358499.3:n.71-453_71-451del
ENST00000369489.9:c.71-453_71-451del	ENSP00000358501.5:n.71-453_71-451del
ENST00000457047.6:c.71-453_71-451del	ENSP00000409080.2:n.71-453_71-451del
ENST00000464088.5:c.71-453_71-451del	ENSP00000432773.1:n.71-453_71-451del
NM_001144822.1:c.71-453_71-451del	NP_001138294.1:n.71-453_71-451del
NM_001779.2:c.71-453_71-451del	NP_001770.1:n.71-453_71-451del
NR_026665.1:n.192-453_192-451del
XR_947739.1:n.210+231_210+233del
XR_947740.1:n.210+231_210+233del
XM_017002869.2:c.71-453_71-451del	XP_016858358.1:n.71-453_71-451del
NM_001779.3:c.71-453_71-451del MANE Select	NP_001770.1:n.71-453_71-451del
NR_026665.2:n.125-453_125-451del
NM_001144822.2:c.71-453_71-451del	NP_001138294.1:n.71-453_71-451del