Canonical Allele Identifier: CA318088645
Gene: CXADR HGNC NCBI

Linked Data

dbSNP Id: rs939628866

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17569847T>C , CM000683.2:g.17569847T>C GRCh38
NC_000021.8:g.18942165T>C , CM000683.1:g.18942165T>C GRCh37
NC_000021.7:g.17864036T>C NCBI36
NG_029458.1:g.61942T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284878.12:c.*4155T>C MANE Select ENSP00000284878.7:n.*4155T>C
ENST00000284878.11:c.*4155T>C ENSP00000284878.7:n.*4155T>C
ENST00000400169.1:c.1017+4236T>C ENSP00000383033.1:n.1017+4236T>C
NM_001207063.1:c.*4232T>C NP_001193992.1:n.*4232T>C
NM_001207064.1:c.*4232T>C NP_001193993.1:n.*4232T>C
NM_001207065.1:c.*4360T>C NP_001193994.1:n.*4360T>C
NM_001207066.1:c.1017+4236T>C NP_001193995.1:n.1017+4236T>C
NM_001338.4:c.*4155T>C NP_001329.1:n.*4155T>C
XM_011529475.1:c.1017+4236T>C XP_011527777.1:n.1017+4236T>C
XM_011529476.1:c.1017+4236T>C XP_011527778.1:n.1017+4236T>C
XM_011529477.1:c.755+4236T>C XP_011527779.1:n.755+4236T>C
XM_011529478.1:c.755+4236T>C XP_011527780.1:n.755+4236T>C
XM_011529479.1:c.755+4236T>C XP_011527781.1:n.755+4236T>C
XM_011529476.2:c.1017+4236T>C XP_011527778.1:n.1017+4236T>C
XM_011529477.2:c.755+4236T>C XP_011527779.1:n.755+4236T>C
XM_011529478.2:c.755+4236T>C XP_011527780.1:n.755+4236T>C
XR_001754814.1:n.1131+4236T>C
NM_001338.5:c.*4155T>C MANE Select NP_001329.1:n.*4155T>C
NM_001207063.2:c.*4232T>C NP_001193992.1:n.*4232T>C
NM_001207064.2:c.*4232T>C NP_001193993.1:n.*4232T>C
NM_001207065.2:c.*4360T>C NP_001193994.1:n.*4360T>C
NM_001207066.2:c.1017+4236T>C NP_001193995.1:n.1017+4236T>C