Canonical Allele Identifier: CA2520496889
Gene: CXADR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17569930_17569931del , CM000683.2:g.17569930_17569931del GRCh38
NC_000021.8:g.18942248_18942249del , CM000683.1:g.18942248_18942249del GRCh37
NC_000021.7:g.17864119_17864120del NCBI36
NG_029458.1:g.62025_62026del

Transcript Alleles

HGVS Amino-acid change
ENST00000284878.12:c.*4238_*4239del MANE Select ENSP00000284878.7:n.*4238_*4239del
ENST00000284878.11:c.*4238_*4239del ENSP00000284878.7:n.*4238_*4239del
ENST00000400169.1:c.1017+4319_1017+4320del ENSP00000383033.1:n.1017+4319_1017+4320de...
NM_001207063.1:c.*4315_*4316del NP_001193992.1:n.*4315_*4316del
NM_001207064.1:c.*4315_*4316del NP_001193993.1:n.*4315_*4316del
NM_001207065.1:c.*4443_*4444del NP_001193994.1:n.*4443_*4444del
NM_001207066.1:c.1017+4319_1017+4320del NP_001193995.1:n.1017+4319_1017+4320del
NM_001338.4:c.*4238_*4239del NP_001329.1:n.*4238_*4239del
XM_011529475.1:c.1017+4319_1017+4320del XP_011527777.1:n.1017+4319_1017+4320del
XM_011529476.1:c.1017+4319_1017+4320del XP_011527778.1:n.1017+4319_1017+4320del
XM_011529477.1:c.755+4319_755+4320del XP_011527779.1:n.755+4319_755+4320del
XM_011529478.1:c.755+4319_755+4320del XP_011527780.1:n.755+4319_755+4320del
XM_011529479.1:c.755+4319_755+4320del XP_011527781.1:n.755+4319_755+4320del
XM_011529476.2:c.1017+4319_1017+4320del XP_011527778.1:n.1017+4319_1017+4320del
XM_011529477.2:c.755+4319_755+4320del XP_011527779.1:n.755+4319_755+4320del
XM_011529478.2:c.755+4319_755+4320del XP_011527780.1:n.755+4319_755+4320del
XR_001754814.1:n.1131+4319_1131+4320del
NM_001338.5:c.*4238_*4239del MANE Select NP_001329.1:n.*4238_*4239del
NM_001207063.2:c.*4315_*4316del NP_001193992.1:n.*4315_*4316del
NM_001207064.2:c.*4315_*4316del NP_001193993.1:n.*4315_*4316del
NM_001207065.2:c.*4443_*4444del NP_001193994.1:n.*4443_*4444del
NM_001207066.2:c.1017+4319_1017+4320del NP_001193995.1:n.1017+4319_1017+4320del