Canonical Allele Identifier: CA2379412269

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17570107_17570109delinsCCT , CM000683.2:g.17570107_17570109delinsCCT	GRCh38
NC_000021.8:g.18942425_18942427delinsCCT , CM000683.1:g.18942425_18942427delinsCCT	GRCh37
NC_000021.7:g.17864296_17864298delinsCCT	NCBI36
NG_029458.1:g.62202_62204delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400169.1:c.1017+4496_1017+4498delinsCCT	ENSP00000383033.1:n.1017+4496_1017+4498delinsCCT
NM_001207063.1:c.*4492_*4494delinsCCT	NP_001193992.1:n.*4492_*4494delinsCCT
NM_001207064.1:c.*4492_*4494delinsCCT	NP_001193993.1:n.*4492_*4494delinsCCT
NM_001207065.1:c.*4620_*4622delinsCCT	NP_001193994.1:n.*4620_*4622delinsCCT
NM_001207066.1:c.1017+4496_1017+4498delinsCCT	NP_001193995.1:n.1017+4496_1017+4498delinsCCT
NM_001338.4:c.*4415_*4417delinsCCT	NP_001329.1:n.*4415_*4417delinsCCT
XM_011529475.1:c.1017+4496_1017+4498delinsCCT	XP_011527777.1:n.1017+4496_1017+4498delinsCCT
XM_011529476.1:c.1017+4496_1017+4498delinsCCT	XP_011527778.1:n.1017+4496_1017+4498delinsCCT
XM_011529477.1:c.755+4496_755+4498delinsCCT	XP_011527779.1:n.755+4496_755+4498delinsCCT
XM_011529478.1:c.755+4496_755+4498delinsCCT	XP_011527780.1:n.755+4496_755+4498delinsCCT
XM_011529479.1:c.755+4496_755+4498delinsCCT	XP_011527781.1:n.755+4496_755+4498delinsCCT
XM_011529476.2:c.1017+4496_1017+4498delinsCCT	XP_011527778.1:n.1017+4496_1017+4498delinsCCT
XM_011529477.2:c.755+4496_755+4498delinsCCT	XP_011527779.1:n.755+4496_755+4498delinsCCT
XM_011529478.2:c.755+4496_755+4498delinsCCT	XP_011527780.1:n.755+4496_755+4498delinsCCT
XR_001754814.1:n.1131+4496_1131+4498delinsCCT
NM_001207066.2:c.1017+4496_1017+4498delinsCCT	NP_001193995.1:n.1017+4496_1017+4498delinsCCT