Canonical Allele Identifier: CA1191068876

Gene: CD58

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116544975A= , CM000663.2:g.116544975A=	GRCh38
NC_000001.10:g.117087597A= , CM000663.1:g.117087597A=	GRCh37
NC_000001.9:g.116889120A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369489.10:c.71-371T= MANE Select	ENSP00000358501.5:n.71-371T=
ENST00000369487.3:c.71-371T=	ENSP00000358499.3:n.71-371T=
ENST00000369489.9:c.71-371T=	ENSP00000358501.5:n.71-371T=
ENST00000457047.6:c.71-371T=	ENSP00000409080.2:n.71-371T=
ENST00000464088.5:c.71-371T=	ENSP00000432773.1:n.71-371T=
NM_001144822.1:c.71-371T=	NP_001138294.1:n.71-371T=
NM_001779.2:c.71-371T=	NP_001770.1:n.71-371T=
NR_026665.1:n.192-371T=
XR_947739.1:n.210+151A=
XR_947740.1:n.210+151A=
XM_017002869.2:c.71-371T=	XP_016858358.1:n.71-371T=
NM_001779.3:c.71-371T= MANE Select	NP_001770.1:n.71-371T=
NR_026665.2:n.125-371T=
NM_001144822.2:c.71-371T=	NP_001138294.1:n.71-371T=