Canonical Allele Identifier: CA2501626061

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17570040_17570041insCC , CM000683.2:g.17570040_17570041insCC	GRCh38
NC_000021.8:g.18942358_18942359insCC , CM000683.1:g.18942358_18942359insCC	GRCh37
NC_000021.7:g.17864229_17864230insCC	NCBI36
NG_029458.1:g.62135_62136insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284878.12:c.*4348_*4349insCC MANE Select	ENSP00000284878.7:n.*4348_*4349insCC
ENST00000284878.11:c.*4348_*4349insCC	ENSP00000284878.7:n.*4348_*4349insCC
ENST00000400169.1:c.1017+4429_1017+4430insCC	ENSP00000383033.1:n.1017+4429_1017+4430insCC
NM_001207063.1:c.*4425_*4426insCC	NP_001193992.1:n.*4425_*4426insCC
NM_001207064.1:c.*4425_*4426insCC	NP_001193993.1:n.*4425_*4426insCC
NM_001207065.1:c.*4553_*4554insCC	NP_001193994.1:n.*4553_*4554insCC
NM_001207066.1:c.1017+4429_1017+4430insCC	NP_001193995.1:n.1017+4429_1017+4430insCC
NM_001338.4:c.*4348_*4349insCC	NP_001329.1:n.*4348_*4349insCC
XM_011529475.1:c.1017+4429_1017+4430insCC	XP_011527777.1:n.1017+4429_1017+4430insCC
XM_011529476.1:c.1017+4429_1017+4430insCC	XP_011527778.1:n.1017+4429_1017+4430insCC
XM_011529477.1:c.755+4429_755+4430insCC	XP_011527779.1:n.755+4429_755+4430insCC
XM_011529478.1:c.755+4429_755+4430insCC	XP_011527780.1:n.755+4429_755+4430insCC
XM_011529479.1:c.755+4429_755+4430insCC	XP_011527781.1:n.755+4429_755+4430insCC
XM_011529476.2:c.1017+4429_1017+4430insCC	XP_011527778.1:n.1017+4429_1017+4430insCC
XM_011529477.2:c.755+4429_755+4430insCC	XP_011527779.1:n.755+4429_755+4430insCC
XM_011529478.2:c.755+4429_755+4430insCC	XP_011527780.1:n.755+4429_755+4430insCC
XR_001754814.1:n.1131+4429_1131+4430insCC
NM_001338.5:c.*4348_*4349insCC MANE Select	NP_001329.1:n.*4348_*4349insCC
NM_001207063.2:c.*4425_*4426insCC	NP_001193992.1:n.*4425_*4426insCC
NM_001207064.2:c.*4425_*4426insCC	NP_001193993.1:n.*4425_*4426insCC
NM_001207065.2:c.*4553_*4554insCC	NP_001193994.1:n.*4553_*4554insCC
NM_001207066.2:c.1017+4429_1017+4430insCC	NP_001193995.1:n.1017+4429_1017+4430insCC