Canonical Allele Identifier: CA525440758

Gene: CD58

Linked Data

• dbSNP Id: rs1402378369
• gnomAD v2: 1-117087612-C-G
• gnomAD v3: 1-116544990-C-G
• gnomAD v4: 1-116544990-C-G
• MyVariant Identifiers: chr1:g.117087612C>G (hg19) ; chr1:g.116544990C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116544990C>G , CM000663.2:g.116544990C>G	GRCh38
NC_000001.10:g.117087612C>G , CM000663.1:g.117087612C>G	GRCh37
NC_000001.9:g.116889135C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369489.10:c.71-386G>C MANE Select	ENSP00000358501.5:n.71-386G>C
ENST00000369487.3:c.71-386G>C	ENSP00000358499.3:n.71-386G>C
ENST00000369489.9:c.71-386G>C	ENSP00000358501.5:n.71-386G>C
ENST00000457047.6:c.71-386G>C	ENSP00000409080.2:n.71-386G>C
ENST00000464088.5:c.71-386G>C	ENSP00000432773.1:n.71-386G>C
NM_001144822.1:c.71-386G>C	NP_001138294.1:n.71-386G>C
NM_001779.2:c.71-386G>C	NP_001770.1:n.71-386G>C
NR_026665.1:n.192-386G>C
XR_947739.1:n.210+166C>G
XR_947740.1:n.210+166C>G
XM_017002869.2:c.71-386G>C	XP_016858358.1:n.71-386G>C
NM_001779.3:c.71-386G>C MANE Select	NP_001770.1:n.71-386G>C
NR_026665.2:n.125-386G>C
NM_001144822.2:c.71-386G>C	NP_001138294.1:n.71-386G>C