Canonical Allele Identifier: CA1139872052

Gene: CD58 MIR548AC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116560027C= , CM000663.2:g.116560027C=	GRCh38
NC_000001.10:g.117102649C= , CM000663.1:g.117102649C=	GRCh37
NC_000001.9:g.116904172C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001779.3:c.70+10876G= (CD58) MANE Select	NP_001770.1:n.70+10876G=
ENST00000369489.10:c.70+10876G= (CD58) MANE Select	ENSP00000358501.5:n.70+10876G=
NM_001144822.1:c.70+10876G= (CD58)	NP_001138294.1:n.70+10876G=
NM_001144822.2:c.70+10876G= (CD58)	NP_001138294.1:n.70+10876G=
NM_001779.2:c.70+10876G= (CD58)	NP_001770.1:n.70+10876G=
NR_026665.1:n.191+10876G= (CD58)
NR_026665.2:n.124+10876G= (CD58)
NR_039621.1:n.85G= (MIR548AC)
ENST00000369487.3:c.70+10876G= (CD58)	ENSP00000358499.3:n.70+10876G=
ENST00000369489.9:c.70+10876G= (CD58)	ENSP00000358501.5:n.70+10876G=
ENST00000457047.6:c.70+10876G= (CD58)	ENSP00000409080.2:n.70+10876G=
ENST00000464088.5:c.70+10876G= (CD58)	ENSP00000432773.1:n.70+10876G=
XM_017002869.2:c.70+10876G= (CD58)	XP_016858358.1:n.70+10876G=