Canonical Allele Identifier: CA1191068920

Gene: CD58

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116545092_116545096delinsAAAGG , CM000663.2:g.116545092_116545096delinsAAAGG	GRCh38
NC_000001.10:g.117087714_117087718delinsAAAGG , CM000663.1:g.117087714_117087718delinsAAAGG	GRCh37
NC_000001.9:g.116889237_116889241delinsAAAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.71-492_71-488delinsCCTTT MANE Select	ENSP00000358501.5:n.71-492_71-488delinsCCTTT
ENST00000369487.3:c.71-492_71-488delinsCCTTT	ENSP00000358499.3:n.71-492_71-488delinsCCTTT
ENST00000369489.9:c.71-492_71-488delinsCCTTT	ENSP00000358501.5:n.71-492_71-488delinsCCTTT
ENST00000457047.6:c.71-492_71-488delinsCCTTT	ENSP00000409080.2:n.71-492_71-488delinsCCTTT
ENST00000464088.5:c.71-492_71-488delinsCCTTT	ENSP00000432773.1:n.71-492_71-488delinsCCTTT
NM_001144822.1:c.71-492_71-488delinsCCTTT	NP_001138294.1:n.71-492_71-488delinsCCTTT
NM_001779.2:c.71-492_71-488delinsCCTTT	NP_001770.1:n.71-492_71-488delinsCCTTT
NR_026665.1:n.192-492_192-488delinsCCTTT
XR_947739.1:n.210+268_210+272delinsAAAGG
XR_947740.1:n.210+268_210+272delinsAAAGG
XM_017002869.2:c.71-492_71-488delinsCCTTT	XP_016858358.1:n.71-492_71-488delinsCCTTT
NM_001779.3:c.71-492_71-488delinsCCTTT MANE Select	NP_001770.1:n.71-492_71-488delinsCCTTT
NR_026665.2:n.125-492_125-488delinsCCTTT
NM_001144822.2:c.71-492_71-488delinsCCTTT	NP_001138294.1:n.71-492_71-488delinsCCTTT