Canonical Allele Identifier: CA2379412085

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17569661_17569668delinsACCCCAGC , CM000683.2:g.17569661_17569668delinsACCCCAGC	GRCh38
NC_000021.8:g.18941979_18941986delinsACCCCAGC , CM000683.1:g.18941979_18941986delinsACCCCAGC	GRCh37
NC_000021.7:g.17863850_17863857delinsACCCCAGC	NCBI36
NG_029458.1:g.61756_61763delinsACCCCAGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000284878.12:c.*3969_*3976delinsACCCCAGC MANE Select	ENSP00000284878.7:n.*3969_*3976delinsACCCCAGC
ENST00000284878.11:c.*3969_*3976delinsACCCCAGC	ENSP00000284878.7:n.*3969_*3976delinsACCCCAGC
ENST00000400169.1:c.1017+4050_1017+4057delinsACCCCAGC	ENSP00000383033.1:n.1017+4050_1017+4057delinsACCCCAGC
NM_001207063.1:c.*4046_*4053delinsACCCCAGC	NP_001193992.1:n.*4046_*4053delinsACCCCAGC
NM_001207064.1:c.*4046_*4053delinsACCCCAGC	NP_001193993.1:n.*4046_*4053delinsACCCCAGC
NM_001207065.1:c.*4174_*4181delinsACCCCAGC	NP_001193994.1:n.*4174_*4181delinsACCCCAGC
NM_001207066.1:c.1017+4050_1017+4057delinsACCCCAGC	NP_001193995.1:n.1017+4050_1017+4057delinsACCCCAGC
NM_001338.4:c.*3969_*3976delinsACCCCAGC	NP_001329.1:n.*3969_*3976delinsACCCCAGC
XM_011529475.1:c.1017+4050_1017+4057delinsACCCCAGC	XP_011527777.1:n.1017+4050_1017+4057delinsACCCCAGC
XM_011529476.1:c.1017+4050_1017+4057delinsACCCCAGC	XP_011527778.1:n.1017+4050_1017+4057delinsACCCCAGC
XM_011529477.1:c.755+4050_755+4057delinsACCCCAGC	XP_011527779.1:n.755+4050_755+4057delinsACCCCAGC
XM_011529478.1:c.755+4050_755+4057delinsACCCCAGC	XP_011527780.1:n.755+4050_755+4057delinsACCCCAGC
XM_011529479.1:c.755+4050_755+4057delinsACCCCAGC	XP_011527781.1:n.755+4050_755+4057delinsACCCCAGC
XM_011529476.2:c.1017+4050_1017+4057delinsACCCCAGC	XP_011527778.1:n.1017+4050_1017+4057delinsACCCCAGC
XM_011529477.2:c.755+4050_755+4057delinsACCCCAGC	XP_011527779.1:n.755+4050_755+4057delinsACCCCAGC
XM_011529478.2:c.755+4050_755+4057delinsACCCCAGC	XP_011527780.1:n.755+4050_755+4057delinsACCCCAGC
XR_001754814.1:n.1131+4050_1131+4057delinsACCCCAGC
NM_001338.5:c.*3969_*3976delinsACCCCAGC MANE Select	NP_001329.1:n.*3969_*3976delinsACCCCAGC
NM_001207063.2:c.*4046_*4053delinsACCCCAGC	NP_001193992.1:n.*4046_*4053delinsACCCCAGC
NM_001207064.2:c.*4046_*4053delinsACCCCAGC	NP_001193993.1:n.*4046_*4053delinsACCCCAGC
NM_001207065.2:c.*4174_*4181delinsACCCCAGC	NP_001193994.1:n.*4174_*4181delinsACCCCAGC
NM_001207066.2:c.1017+4050_1017+4057delinsACCCCAGC	NP_001193995.1:n.1017+4050_1017+4057delinsACCCCAGC