Canonical Allele Identifier: CA2379412207
Gene: CXADR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17569962G= , CM000683.2:g.17569962G= GRCh38
NC_000021.8:g.18942280G= , CM000683.1:g.18942280G= GRCh37
NC_000021.7:g.17864151G= NCBI36
NG_029458.1:g.62057G=

Transcript Alleles

HGVS Amino-acid change
ENST00000284878.12:c.*4270G= MANE Select ENSP00000284878.7:n.*4270G=
ENST00000284878.11:c.*4270G= ENSP00000284878.7:n.*4270G=
ENST00000400169.1:c.1017+4351G= ENSP00000383033.1:n.1017+4351G=
NM_001207063.1:c.*4347G= NP_001193992.1:n.*4347G=
NM_001207064.1:c.*4347G= NP_001193993.1:n.*4347G=
NM_001207065.1:c.*4475G= NP_001193994.1:n.*4475G=
NM_001207066.1:c.1017+4351G= NP_001193995.1:n.1017+4351G=
NM_001338.4:c.*4270G= NP_001329.1:n.*4270G=
XM_011529475.1:c.1017+4351G= XP_011527777.1:n.1017+4351G=
XM_011529476.1:c.1017+4351G= XP_011527778.1:n.1017+4351G=
XM_011529477.1:c.755+4351G= XP_011527779.1:n.755+4351G=
XM_011529478.1:c.755+4351G= XP_011527780.1:n.755+4351G=
XM_011529479.1:c.755+4351G= XP_011527781.1:n.755+4351G=
XM_011529476.2:c.1017+4351G= XP_011527778.1:n.1017+4351G=
XM_011529477.2:c.755+4351G= XP_011527779.1:n.755+4351G=
XM_011529478.2:c.755+4351G= XP_011527780.1:n.755+4351G=
XR_001754814.1:n.1131+4351G=
NM_001338.5:c.*4270G= MANE Select NP_001329.1:n.*4270G=
NM_001207063.2:c.*4347G= NP_001193992.1:n.*4347G=
NM_001207064.2:c.*4347G= NP_001193993.1:n.*4347G=
NM_001207065.2:c.*4475G= NP_001193994.1:n.*4475G=
NM_001207066.2:c.1017+4351G= NP_001193995.1:n.1017+4351G=