Canonical Allele Identifier: CA2379412217
Gene: CXADR HGNC NCBI

Linked Data

dbSNP Id: rs1328727964

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17569976G>T , CM000683.2:g.17569976G>T GRCh38
NC_000021.8:g.18942294G>T , CM000683.1:g.18942294G>T GRCh37
NC_000021.7:g.17864165G>T NCBI36
NG_029458.1:g.62071G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000284878.12:c.*4284G>T MANE Select ENSP00000284878.7:n.*4284G>T
ENST00000284878.11:c.*4284G>T ENSP00000284878.7:n.*4284G>T
ENST00000400169.1:c.1017+4365G>T ENSP00000383033.1:n.1017+4365G>T
NM_001207063.1:c.*4361G>T NP_001193992.1:n.*4361G>T
NM_001207064.1:c.*4361G>T NP_001193993.1:n.*4361G>T
NM_001207065.1:c.*4489G>T NP_001193994.1:n.*4489G>T
NM_001207066.1:c.1017+4365G>T NP_001193995.1:n.1017+4365G>T
NM_001338.4:c.*4284G>T NP_001329.1:n.*4284G>T
XM_011529475.1:c.1017+4365G>T XP_011527777.1:n.1017+4365G>T
XM_011529476.1:c.1017+4365G>T XP_011527778.1:n.1017+4365G>T
XM_011529477.1:c.755+4365G>T XP_011527779.1:n.755+4365G>T
XM_011529478.1:c.755+4365G>T XP_011527780.1:n.755+4365G>T
XM_011529479.1:c.755+4365G>T XP_011527781.1:n.755+4365G>T
XM_011529476.2:c.1017+4365G>T XP_011527778.1:n.1017+4365G>T
XM_011529477.2:c.755+4365G>T XP_011527779.1:n.755+4365G>T
XM_011529478.2:c.755+4365G>T XP_011527780.1:n.755+4365G>T
XR_001754814.1:n.1131+4365G>T
NM_001338.5:c.*4284G>T MANE Select NP_001329.1:n.*4284G>T
NM_001207063.2:c.*4361G>T NP_001193992.1:n.*4361G>T
NM_001207064.2:c.*4361G>T NP_001193993.1:n.*4361G>T
NM_001207065.2:c.*4489G>T NP_001193994.1:n.*4489G>T
NM_001207066.2:c.1017+4365G>T NP_001193995.1:n.1017+4365G>T