Canonical Allele Identifier: CA2542948652

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17570033_17570034insGC , CM000683.2:g.17570033_17570034insGC	GRCh38
NC_000021.8:g.18942351_18942352insGC , CM000683.1:g.18942351_18942352insGC	GRCh37
NC_000021.7:g.17864222_17864223insGC	NCBI36
NG_029458.1:g.62128_62129insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284878.12:c.*4341_*4342insGC MANE Select	ENSP00000284878.7:n.*4341_*4342insGC
ENST00000284878.11:c.*4341_*4342insGC	ENSP00000284878.7:n.*4341_*4342insGC
ENST00000400169.1:c.1017+4422_1017+4423insGC	ENSP00000383033.1:n.1017+4422_1017+4423insGC
NM_001207063.1:c.*4418_*4419insGC	NP_001193992.1:n.*4418_*4419insGC
NM_001207064.1:c.*4418_*4419insGC	NP_001193993.1:n.*4418_*4419insGC
NM_001207065.1:c.*4546_*4547insGC	NP_001193994.1:n.*4546_*4547insGC
NM_001207066.1:c.1017+4422_1017+4423insGC	NP_001193995.1:n.1017+4422_1017+4423insGC
NM_001338.4:c.*4341_*4342insGC	NP_001329.1:n.*4341_*4342insGC
XM_011529475.1:c.1017+4422_1017+4423insGC	XP_011527777.1:n.1017+4422_1017+4423insGC
XM_011529476.1:c.1017+4422_1017+4423insGC	XP_011527778.1:n.1017+4422_1017+4423insGC
XM_011529477.1:c.755+4422_755+4423insGC	XP_011527779.1:n.755+4422_755+4423insGC
XM_011529478.1:c.755+4422_755+4423insGC	XP_011527780.1:n.755+4422_755+4423insGC
XM_011529479.1:c.755+4422_755+4423insGC	XP_011527781.1:n.755+4422_755+4423insGC
XM_011529476.2:c.1017+4422_1017+4423insGC	XP_011527778.1:n.1017+4422_1017+4423insGC
XM_011529477.2:c.755+4422_755+4423insGC	XP_011527779.1:n.755+4422_755+4423insGC
XM_011529478.2:c.755+4422_755+4423insGC	XP_011527780.1:n.755+4422_755+4423insGC
XR_001754814.1:n.1131+4422_1131+4423insGC
NM_001338.5:c.*4341_*4342insGC MANE Select	NP_001329.1:n.*4341_*4342insGC
NM_001207063.2:c.*4418_*4419insGC	NP_001193992.1:n.*4418_*4419insGC
NM_001207064.2:c.*4418_*4419insGC	NP_001193993.1:n.*4418_*4419insGC
NM_001207065.2:c.*4546_*4547insGC	NP_001193994.1:n.*4546_*4547insGC
NM_001207066.2:c.1017+4422_1017+4423insGC	NP_001193995.1:n.1017+4422_1017+4423insGC