Canonical Allele Identifier: CA1191074082

Gene: CD58

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116558335A>C , CM000663.2:g.116558335A>C	GRCh38
NC_000001.10:g.117100957A>C , CM000663.1:g.117100957A>C	GRCh37
NC_000001.9:g.116902480A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369489.10:c.70+12568T>G MANE Select	ENSP00000358501.5:n.70+12568T>G
ENST00000369487.3:c.70+12568T>G	ENSP00000358499.3:n.70+12568T>G
ENST00000369489.9:c.70+12568T>G	ENSP00000358501.5:n.70+12568T>G
ENST00000457047.6:c.70+12568T>G	ENSP00000409080.2:n.70+12568T>G
ENST00000464088.5:c.70+12568T>G	ENSP00000432773.1:n.70+12568T>G
NM_001144822.1:c.70+12568T>G	NP_001138294.1:n.70+12568T>G
NM_001779.2:c.70+12568T>G	NP_001770.1:n.70+12568T>G
NR_026665.1:n.191+12568T>G
XM_017002869.2:c.70+12568T>G	XP_016858358.1:n.70+12568T>G
NM_001779.3:c.70+12568T>G MANE Select	NP_001770.1:n.70+12568T>G
NR_026665.2:n.124+12568T>G
NM_001144822.2:c.70+12568T>G	NP_001138294.1:n.70+12568T>G