Canonical Allele Identifier: CA2577489743

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17569788_17569789del , CM000683.2:g.17569788_17569789del	GRCh38
NC_000021.8:g.18942106_18942107del , CM000683.1:g.18942106_18942107del	GRCh37
NC_000021.7:g.17863977_17863978del	NCBI36
NG_029458.1:g.61883_61884del

Transcript Alleles

HGVS	Amino-acid change
ENST00000284878.12:c.*4096_*4097del MANE Select	ENSP00000284878.7:n.*4096_*4097del
ENST00000284878.11:c.*4096_*4097del	ENSP00000284878.7:n.*4096_*4097del
ENST00000400169.1:c.1017+4177_1017+4178del	ENSP00000383033.1:n.1017+4177_1017+4178de...
NM_001207063.1:c.*4173_*4174del	NP_001193992.1:n.*4173_*4174del
NM_001207064.1:c.*4173_*4174del	NP_001193993.1:n.*4173_*4174del
NM_001207065.1:c.*4301_*4302del	NP_001193994.1:n.*4301_*4302del
NM_001207066.1:c.1017+4177_1017+4178del	NP_001193995.1:n.1017+4177_1017+4178del
NM_001338.4:c.*4096_*4097del	NP_001329.1:n.*4096_*4097del
XM_011529475.1:c.1017+4177_1017+4178del	XP_011527777.1:n.1017+4177_1017+4178del
XM_011529476.1:c.1017+4177_1017+4178del	XP_011527778.1:n.1017+4177_1017+4178del
XM_011529477.1:c.755+4177_755+4178del	XP_011527779.1:n.755+4177_755+4178del
XM_011529478.1:c.755+4177_755+4178del	XP_011527780.1:n.755+4177_755+4178del
XM_011529479.1:c.755+4177_755+4178del	XP_011527781.1:n.755+4177_755+4178del
XM_011529476.2:c.1017+4177_1017+4178del	XP_011527778.1:n.1017+4177_1017+4178del
XM_011529477.2:c.755+4177_755+4178del	XP_011527779.1:n.755+4177_755+4178del
XM_011529478.2:c.755+4177_755+4178del	XP_011527780.1:n.755+4177_755+4178del
XR_001754814.1:n.1131+4177_1131+4178del
NM_001338.5:c.*4096_*4097del MANE Select	NP_001329.1:n.*4096_*4097del
NM_001207063.2:c.*4173_*4174del	NP_001193992.1:n.*4173_*4174del
NM_001207064.2:c.*4173_*4174del	NP_001193993.1:n.*4173_*4174del
NM_001207065.2:c.*4301_*4302del	NP_001193994.1:n.*4301_*4302del
NM_001207066.2:c.1017+4177_1017+4178del	NP_001193995.1:n.1017+4177_1017+4178del