Canonical Allele Identifier: CA419911729

Gene: CD58 NAP1L4P1

Linked Data

• MyVariant Identifiers: chr1:g.117076466C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116533844C>A , CM000663.2:g.116533844C>A	GRCh38
NC_000001.10:g.117076466C>A , CM000663.1:g.117076466C>A	GRCh37
NC_000001.9:g.116877989C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.628+2121G>T (CD58) MANE Select	ENSP00000358501.5:n.628+2121G>T
ENST00000319092.5:n.249G>T (NAP1L4P1)
ENST00000369487.3:c.628+2121G>T (CD58)	ENSP00000358499.3:n.628+2121G>T
ENST00000369489.9:c.628+2121G>T (CD58)	ENSP00000358501.5:n.628+2121G>T
ENST00000457047.6:c.628+2121G>T (CD58)	ENSP00000409080.2:n.628+2121G>T
ENST00000464088.5:c.628+2121G>T (CD58)	ENSP00000432773.1:n.628+2121G>T
ENST00000526981.1:c.280+10467G>T (CD58)	ENSP00000433648.1:n.280+10467G>T
NM_001144822.1:c.628+2121G>T (CD58)	NP_001138294.1:n.628+2121G>T
NM_001779.2:c.628+2121G>T (CD58)	NP_001770.1:n.628+2121G>T
NR_026665.1:n.749+2121G>T (CD58)
XM_017002869.2:c.628+2121G>T (CD58)	XP_016858358.1:n.628+2121G>T
NM_001779.3:c.628+2121G>T (CD58) MANE Select	NP_001770.1:n.628+2121G>T
NR_026665.2:n.682+2121G>T (CD58)
NM_001144822.2:c.628+2121G>T (CD58)	NP_001138294.1:n.628+2121G>T