Canonical Allele Identifier: CA15137433

Gene: CD58

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116561593A>G , CM000663.2:g.116561593A>G	GRCh38
NC_000001.10:g.117104215A>G , CM000663.1:g.117104215A>G	GRCh37
NC_000001.9:g.116905738A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369489.10:c.70+9310T>C MANE Select	ENSP00000358501.5:n.70+9310T>C
ENST00000369487.3:c.70+9310T>C	ENSP00000358499.3:n.70+9310T>C
ENST00000369489.9:c.70+9310T>C	ENSP00000358501.5:n.70+9310T>C
ENST00000457047.6:c.70+9310T>C	ENSP00000409080.2:n.70+9310T>C
ENST00000464088.5:c.70+9310T>C	ENSP00000432773.1:n.70+9310T>C
NM_001144822.1:c.70+9310T>C	NP_001138294.1:n.70+9310T>C
NM_001779.2:c.70+9310T>C	NP_001770.1:n.70+9310T>C
NR_026665.1:n.191+9310T>C
XM_017002869.2:c.70+9310T>C	XP_016858358.1:n.70+9310T>C
NM_001779.3:c.70+9310T>C MANE Select	NP_001770.1:n.70+9310T>C
NR_026665.2:n.124+9310T>C
NM_001144822.2:c.70+9310T>C	NP_001138294.1:n.70+9310T>C