Canonical Allele Identifier: CA2379412130
Gene: CXADR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17569776C= , CM000683.2:g.17569776C= GRCh38
NC_000021.8:g.18942094C= , CM000683.1:g.18942094C= GRCh37
NC_000021.7:g.17863965C= NCBI36
NG_029458.1:g.61871C=

Transcript Alleles

HGVS Amino-acid change
ENST00000284878.12:c.*4084C= MANE Select ENSP00000284878.7:n.*4084C=
ENST00000284878.11:c.*4084C= ENSP00000284878.7:n.*4084C=
ENST00000400169.1:c.1017+4165C= ENSP00000383033.1:n.1017+4165C=
NM_001207063.1:c.*4161C= NP_001193992.1:n.*4161C=
NM_001207064.1:c.*4161C= NP_001193993.1:n.*4161C=
NM_001207065.1:c.*4289C= NP_001193994.1:n.*4289C=
NM_001207066.1:c.1017+4165C= NP_001193995.1:n.1017+4165C=
NM_001338.4:c.*4084C= NP_001329.1:n.*4084C=
XM_011529475.1:c.1017+4165C= XP_011527777.1:n.1017+4165C=
XM_011529476.1:c.1017+4165C= XP_011527778.1:n.1017+4165C=
XM_011529477.1:c.755+4165C= XP_011527779.1:n.755+4165C=
XM_011529478.1:c.755+4165C= XP_011527780.1:n.755+4165C=
XM_011529479.1:c.755+4165C= XP_011527781.1:n.755+4165C=
XM_011529476.2:c.1017+4165C= XP_011527778.1:n.1017+4165C=
XM_011529477.2:c.755+4165C= XP_011527779.1:n.755+4165C=
XM_011529478.2:c.755+4165C= XP_011527780.1:n.755+4165C=
XR_001754814.1:n.1131+4165C=
NM_001338.5:c.*4084C= MANE Select NP_001329.1:n.*4084C=
NM_001207063.2:c.*4161C= NP_001193992.1:n.*4161C=
NM_001207064.2:c.*4161C= NP_001193993.1:n.*4161C=
NM_001207065.2:c.*4289C= NP_001193994.1:n.*4289C=
NM_001207066.2:c.1017+4165C= NP_001193995.1:n.1017+4165C=