Canonical Allele Identifier: CA2577489758

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17570005_17570011del , CM000683.2:g.17570005_17570011del	GRCh38
NC_000021.8:g.18942323_18942329del , CM000683.1:g.18942323_18942329del	GRCh37
NC_000021.7:g.17864194_17864200del	NCBI36
NG_029458.1:g.62100_62106del

Transcript Alleles

HGVS	Amino-acid change
ENST00000284878.12:c.*4313_*4319del MANE Select	ENSP00000284878.7:n.*4313_*4319del
ENST00000284878.11:c.*4313_*4319del	ENSP00000284878.7:n.*4313_*4319del
ENST00000400169.1:c.1017+4394_1017+4400del	ENSP00000383033.1:n.1017+4394_1017+4400de...
NM_001207063.1:c.*4390_*4396del	NP_001193992.1:n.*4390_*4396del
NM_001207064.1:c.*4390_*4396del	NP_001193993.1:n.*4390_*4396del
NM_001207065.1:c.*4518_*4524del	NP_001193994.1:n.*4518_*4524del
NM_001207066.1:c.1017+4394_1017+4400del	NP_001193995.1:n.1017+4394_1017+4400del
NM_001338.4:c.*4313_*4319del	NP_001329.1:n.*4313_*4319del
XM_011529475.1:c.1017+4394_1017+4400del	XP_011527777.1:n.1017+4394_1017+4400del
XM_011529476.1:c.1017+4394_1017+4400del	XP_011527778.1:n.1017+4394_1017+4400del
XM_011529477.1:c.755+4394_755+4400del	XP_011527779.1:n.755+4394_755+4400del
XM_011529478.1:c.755+4394_755+4400del	XP_011527780.1:n.755+4394_755+4400del
XM_011529479.1:c.755+4394_755+4400del	XP_011527781.1:n.755+4394_755+4400del
XM_011529476.2:c.1017+4394_1017+4400del	XP_011527778.1:n.1017+4394_1017+4400del
XM_011529477.2:c.755+4394_755+4400del	XP_011527779.1:n.755+4394_755+4400del
XM_011529478.2:c.755+4394_755+4400del	XP_011527780.1:n.755+4394_755+4400del
XR_001754814.1:n.1131+4394_1131+4400del
NM_001338.5:c.*4313_*4319del MANE Select	NP_001329.1:n.*4313_*4319del
NM_001207063.2:c.*4390_*4396del	NP_001193992.1:n.*4390_*4396del
NM_001207064.2:c.*4390_*4396del	NP_001193993.1:n.*4390_*4396del
NM_001207065.2:c.*4518_*4524del	NP_001193994.1:n.*4518_*4524del
NM_001207066.2:c.1017+4394_1017+4400del	NP_001193995.1:n.1017+4394_1017+4400del