Canonical Allele Identifier: CA318088649
Gene: CXADR HGNC NCBI

Linked Data

dbSNP Id: rs946226003

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17569862C>A , CM000683.2:g.17569862C>A GRCh38
NC_000021.8:g.18942180C>A , CM000683.1:g.18942180C>A GRCh37
NC_000021.7:g.17864051C>A NCBI36
NG_029458.1:g.61957C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000284878.12:c.*4170C>A MANE Select ENSP00000284878.7:n.*4170C>A
ENST00000284878.11:c.*4170C>A ENSP00000284878.7:n.*4170C>A
ENST00000400169.1:c.1017+4251C>A ENSP00000383033.1:n.1017+4251C>A
NM_001207063.1:c.*4247C>A NP_001193992.1:n.*4247C>A
NM_001207064.1:c.*4247C>A NP_001193993.1:n.*4247C>A
NM_001207065.1:c.*4375C>A NP_001193994.1:n.*4375C>A
NM_001207066.1:c.1017+4251C>A NP_001193995.1:n.1017+4251C>A
NM_001338.4:c.*4170C>A NP_001329.1:n.*4170C>A
XM_011529475.1:c.1017+4251C>A XP_011527777.1:n.1017+4251C>A
XM_011529476.1:c.1017+4251C>A XP_011527778.1:n.1017+4251C>A
XM_011529477.1:c.755+4251C>A XP_011527779.1:n.755+4251C>A
XM_011529478.1:c.755+4251C>A XP_011527780.1:n.755+4251C>A
XM_011529479.1:c.755+4251C>A XP_011527781.1:n.755+4251C>A
XM_011529476.2:c.1017+4251C>A XP_011527778.1:n.1017+4251C>A
XM_011529477.2:c.755+4251C>A XP_011527779.1:n.755+4251C>A
XM_011529478.2:c.755+4251C>A XP_011527780.1:n.755+4251C>A
XR_001754814.1:n.1131+4251C>A
NM_001338.5:c.*4170C>A MANE Select NP_001329.1:n.*4170C>A
NM_001207063.2:c.*4247C>A NP_001193992.1:n.*4247C>A
NM_001207064.2:c.*4247C>A NP_001193993.1:n.*4247C>A
NM_001207065.2:c.*4375C>A NP_001193994.1:n.*4375C>A
NM_001207066.2:c.1017+4251C>A NP_001193995.1:n.1017+4251C>A