Canonical Allele Identifier: CA1191064643

Gene: CD58 NAP1L4P1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116533940G= , CM000663.2:g.116533940G=	GRCh38
NC_000001.10:g.117076562G= , CM000663.1:g.117076562G=	GRCh37
NC_000001.9:g.116878085G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.628+2025C= (CD58) MANE Select	ENSP00000358501.5:n.628+2025C=
ENST00000319092.5:n.153C= (NAP1L4P1)
ENST00000369487.3:c.628+2025C= (CD58)	ENSP00000358499.3:n.628+2025C=
ENST00000369489.9:c.628+2025C= (CD58)	ENSP00000358501.5:n.628+2025C=
ENST00000457047.6:c.628+2025C= (CD58)	ENSP00000409080.2:n.628+2025C=
ENST00000464088.5:c.628+2025C= (CD58)	ENSP00000432773.1:n.628+2025C=
ENST00000526981.1:c.280+10371C= (CD58)	ENSP00000433648.1:n.280+10371C=
NM_001144822.1:c.628+2025C= (CD58)	NP_001138294.1:n.628+2025C=
NM_001779.2:c.628+2025C= (CD58)	NP_001770.1:n.628+2025C=
NR_026665.1:n.749+2025C= (CD58)
XM_017002869.2:c.628+2025C= (CD58)	XP_016858358.1:n.628+2025C=
NM_001779.3:c.628+2025C= (CD58) MANE Select	NP_001770.1:n.628+2025C=
NR_026665.2:n.682+2025C= (CD58)
NM_001144822.2:c.628+2025C= (CD58)	NP_001138294.1:n.628+2025C=