Canonical Allele Identifier: CA14876460
Gene: CXADR HGNC NCBI

Linked Data

dbSNP Id: rs12034

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17569905G>A , CM000683.2:g.17569905G>A GRCh38
NC_000021.8:g.18942223G>A , CM000683.1:g.18942223G>A GRCh37
NC_000021.7:g.17864094G>A NCBI36
NG_029458.1:g.62000G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000284878.12:c.*4213G>A MANE Select ENSP00000284878.7:p.=
ENST00000284878.11:c.*4213G>A ENSP00000284878.7:p.=
ENST00000400169.1:n.1017+4294G>A ENSP00000383033.1:p.=
NM_001207063.1:c.*4290G>A NP_001193992.1:p.=
NM_001207064.1:c.*4290G>A NP_001193993.1:p.=
NM_001207065.1:c.*4418G>A NP_001193994.1:p.=
NM_001207066.1:c.1017+4294G>A NP_001193995.1:p.=
NM_001338.4:c.*4213G>A NP_001329.1:p.=
XM_011529475.1:c.1017+4294G>A XP_011527777.1:p.=
XM_011529476.1:c.1017+4294G>A XP_011527778.1:p.=
XM_011529477.1:c.755+4294G>A XP_011527779.1:p.=
XM_011529478.1:c.755+4294G>A XP_011527780.1:p.=
XM_011529479.1:c.755+4294G>A XP_011527781.1:p.=
XM_011529476.2:c.1017+4294G>A XP_011527778.1:p.=
XM_011529477.2:c.755+4294G>A XP_011527779.1:p.=
XM_011529478.2:c.755+4294G>A XP_011527780.1:p.=
XR_001754814.1:n.1131+4294G>A
NM_001338.5:c.*4213G>A MANE Select NP_001329.1:p.=
NM_001207063.2:c.*4290G>A NP_001193992.1:p.=
NM_001207064.2:c.*4290G>A NP_001193993.1:p.=
NM_001207065.2:c.*4418G>A NP_001193994.1:p.=
NM_001207066.2:c.1017+4294G>A NP_001193995.1:p.=