Canonical Allele Identifier: CA885992994

Gene: CD58

Linked Data

• dbSNP Id: rs1361700614
• MyVariant Identifiers: chr1:g.117087734_117087735insAA (hg19) ; chr1:g.116545112_116545113insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116545114_116545115dup , CM000663.2:g.116545114_116545115dup	GRCh38
NC_000001.10:g.117087736_117087737dup , CM000663.1:g.117087736_117087737dup	GRCh37
NC_000001.9:g.116889259_116889260dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.71-510_71-509dup MANE Select	ENSP00000358501.5:n.71-510_71-509dup
ENST00000369487.3:c.71-510_71-509dup	ENSP00000358499.3:n.71-510_71-509dup
ENST00000369489.9:c.71-510_71-509dup	ENSP00000358501.5:n.71-510_71-509dup
ENST00000457047.6:c.71-510_71-509dup	ENSP00000409080.2:n.71-510_71-509dup
ENST00000464088.5:c.71-510_71-509dup	ENSP00000432773.1:n.71-510_71-509dup
NM_001144822.1:c.71-510_71-509dup	NP_001138294.1:n.71-510_71-509dup
NM_001779.2:c.71-510_71-509dup	NP_001770.1:n.71-510_71-509dup
NR_026665.1:n.192-510_192-509dup
XR_947739.1:n.210+290_210+291dup
XR_947740.1:n.210+290_210+291dup
XM_017002869.2:c.71-510_71-509dup	XP_016858358.1:n.71-510_71-509dup
NM_001779.3:c.71-510_71-509dup MANE Select	NP_001770.1:n.71-510_71-509dup
NR_026665.2:n.125-510_125-509dup
NM_001144822.2:c.71-510_71-509dup	NP_001138294.1:n.71-510_71-509dup