Canonical Allele Identifier: CA636777765

Gene: CXADR

Linked Data

• dbSNP Id: rs1410215434
• gnomAD v2: 21-18942425-CCT-C
• gnomAD v3: 21-17570107-CCT-C
• gnomAD v4: 21-17570107-CCT-C
• MyVariant Identifiers: chr21:g.18942426_18942427del (hg19) ; chr21:g.17570108_17570109del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17570109_17570110del , CM000683.2:g.17570109_17570110del	GRCh38
NC_000021.8:g.18942427_18942428del , CM000683.1:g.18942427_18942428del	GRCh37
NC_000021.7:g.17864298_17864299del	NCBI36
NG_029458.1:g.62204_62205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400169.1:c.1017+4498_1017+4499del	ENSP00000383033.1:n.1017+4498_1017+4499del
NM_001207063.1:c.*4494_*4495del	NP_001193992.1:n.*4494_*4495del
NM_001207064.1:c.*4494_*4495del	NP_001193993.1:n.*4494_*4495del
NM_001207065.1:c.*4622_*4623del	NP_001193994.1:n.*4622_*4623del
NM_001207066.1:c.1017+4498_1017+4499del	NP_001193995.1:n.1017+4498_1017+4499del
NM_001338.4:c.*4417_*4418del	NP_001329.1:n.*4417_*4418del
XM_011529475.1:c.1017+4498_1017+4499del	XP_011527777.1:n.1017+4498_1017+4499del
XM_011529476.1:c.1017+4498_1017+4499del	XP_011527778.1:n.1017+4498_1017+4499del
XM_011529477.1:c.755+4498_755+4499del	XP_011527779.1:n.755+4498_755+4499del
XM_011529478.1:c.755+4498_755+4499del	XP_011527780.1:n.755+4498_755+4499del
XM_011529479.1:c.755+4498_755+4499del	XP_011527781.1:n.755+4498_755+4499del
XM_011529476.2:c.1017+4498_1017+4499del	XP_011527778.1:n.1017+4498_1017+4499del
XM_011529477.2:c.755+4498_755+4499del	XP_011527779.1:n.755+4498_755+4499del
XM_011529478.2:c.755+4498_755+4499del	XP_011527780.1:n.755+4498_755+4499del
XR_001754814.1:n.1131+4498_1131+4499del
NM_001207066.2:c.1017+4498_1017+4499del	NP_001193995.1:n.1017+4498_1017+4499del