Canonical Allele Identifier: CA2654096246
Gene: CXADR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17569827_17569832del , CM000683.2:g.17569827_17569832del GRCh38
NC_000021.8:g.18942145_18942150del , CM000683.1:g.18942145_18942150del GRCh37
NC_000021.7:g.17864016_17864021del NCBI36
NG_029458.1:g.61922_61927del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284878.12:c.*4135_*4140del MANE Select ENSP00000284878.7:n.*4135_*4140del
ENST00000284878.11:c.*4135_*4140del ENSP00000284878.7:n.*4135_*4140del
ENST00000400169.1:c.1017+4216_1017+4221del ENSP00000383033.1:n.1017+4216_1017+4221del
NM_001207063.1:c.*4212_*4217del NP_001193992.1:n.*4212_*4217del
NM_001207064.1:c.*4212_*4217del NP_001193993.1:n.*4212_*4217del
NM_001207065.1:c.*4340_*4345del NP_001193994.1:n.*4340_*4345del
NM_001207066.1:c.1017+4216_1017+4221del NP_001193995.1:n.1017+4216_1017+4221del
NM_001338.4:c.*4135_*4140del NP_001329.1:n.*4135_*4140del
XM_011529475.1:c.1017+4216_1017+4221del XP_011527777.1:n.1017+4216_1017+4221del
XM_011529476.1:c.1017+4216_1017+4221del XP_011527778.1:n.1017+4216_1017+4221del
XM_011529477.1:c.755+4216_755+4221del XP_011527779.1:n.755+4216_755+4221del
XM_011529478.1:c.755+4216_755+4221del XP_011527780.1:n.755+4216_755+4221del
XM_011529479.1:c.755+4216_755+4221del XP_011527781.1:n.755+4216_755+4221del
XM_011529476.2:c.1017+4216_1017+4221del XP_011527778.1:n.1017+4216_1017+4221del
XM_011529477.2:c.755+4216_755+4221del XP_011527779.1:n.755+4216_755+4221del
XM_011529478.2:c.755+4216_755+4221del XP_011527780.1:n.755+4216_755+4221del
XR_001754814.1:n.1131+4216_1131+4221del
NM_001338.5:c.*4135_*4140del MANE Select NP_001329.1:n.*4135_*4140del
NM_001207063.2:c.*4212_*4217del NP_001193992.1:n.*4212_*4217del
NM_001207064.2:c.*4212_*4217del NP_001193993.1:n.*4212_*4217del
NM_001207065.2:c.*4340_*4345del NP_001193994.1:n.*4340_*4345del
NM_001207066.2:c.1017+4216_1017+4221del NP_001193995.1:n.1017+4216_1017+4221del