Canonical Allele Identifier: CA2379412252
Gene: CXADR HGNC NCBI

Linked Data

dbSNP Id: rs2061264567

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.17570057_17570058insG , CM000683.2:g.17570057_17570058insG GRCh38
NC_000021.8:g.18942375_18942376insG , CM000683.1:g.18942375_18942376insG GRCh37
NC_000021.7:g.17864246_17864247insG NCBI36
NG_029458.1:g.62152_62153insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000284878.12:c.*4365_*4366insG MANE Select ENSP00000284878.7:n.*4365_*4366insG
ENST00000284878.11:c.*4365_*4366insG ENSP00000284878.7:n.*4365_*4366insG
ENST00000400169.1:c.1017+4446_1017+4447insG ENSP00000383033.1:n.1017+4446_1017+4447insG
NM_001207063.1:c.*4442_*4443insG NP_001193992.1:n.*4442_*4443insG
NM_001207064.1:c.*4442_*4443insG NP_001193993.1:n.*4442_*4443insG
NM_001207065.1:c.*4570_*4571insG NP_001193994.1:n.*4570_*4571insG
NM_001207066.1:c.1017+4446_1017+4447insG NP_001193995.1:n.1017+4446_1017+4447insG
NM_001338.4:c.*4365_*4366insG NP_001329.1:n.*4365_*4366insG
XM_011529475.1:c.1017+4446_1017+4447insG XP_011527777.1:n.1017+4446_1017+4447insG
XM_011529476.1:c.1017+4446_1017+4447insG XP_011527778.1:n.1017+4446_1017+4447insG
XM_011529477.1:c.755+4446_755+4447insG XP_011527779.1:n.755+4446_755+4447insG
XM_011529478.1:c.755+4446_755+4447insG XP_011527780.1:n.755+4446_755+4447insG
XM_011529479.1:c.755+4446_755+4447insG XP_011527781.1:n.755+4446_755+4447insG
XM_011529476.2:c.1017+4446_1017+4447insG XP_011527778.1:n.1017+4446_1017+4447insG
XM_011529477.2:c.755+4446_755+4447insG XP_011527779.1:n.755+4446_755+4447insG
XM_011529478.2:c.755+4446_755+4447insG XP_011527780.1:n.755+4446_755+4447insG
XR_001754814.1:n.1131+4446_1131+4447insG
NM_001338.5:c.*4365_*4366insG MANE Select NP_001329.1:n.*4365_*4366insG
NM_001207063.2:c.*4442_*4443insG NP_001193992.1:n.*4442_*4443insG
NM_001207064.2:c.*4442_*4443insG NP_001193993.1:n.*4442_*4443insG
NM_001207065.2:c.*4570_*4571insG NP_001193994.1:n.*4570_*4571insG
NM_001207066.2:c.1017+4446_1017+4447insG NP_001193995.1:n.1017+4446_1017+4447insG