Canonical Allele Identifier: CA1025916

Gene: CD58

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116544574T>C , CM000663.2:g.116544574T>C	GRCh38
NC_000001.10:g.117087196T>C , CM000663.1:g.117087196T>C	GRCh37
NC_000001.9:g.116888719T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369489.10:c.101A>G MANE Select	ENSP00000358501.5:p.Tyr34Cys
ENST00000369487.3:c.101A>G	ENSP00000358499.3:p.Tyr34Cys
ENST00000369489.9:c.101A>G	ENSP00000358501.5:p.Tyr34Cys
ENST00000457047.6:c.101A>G	ENSP00000409080.2:p.Tyr34Cys
ENST00000464088.5:c.101A>G	ENSP00000432773.1:p.Tyr34Cys
ENST00000526981.1:c.17A>G	ENSP00000433648.1:p.Tyr6Cys
NM_001144822.1:c.101A>G	NP_001138294.1:p.Tyr34Cys
NM_001779.2:c.101A>G	NP_001770.1:p.Tyr34Cys
NR_026665.1:n.222A>G
XM_017002869.2:c.101A>G	XP_016858358.1:p.Tyr34Cys
NM_001779.3:c.101A>G MANE Select	NP_001770.1:p.Tyr34Cys
NR_026665.2:n.155A>G
NM_001144822.2:c.101A>G	NP_001138294.1:p.Tyr34Cys