Canonical Allele Identifier: CA2654096225

Gene: CXADR

Linked Data

• gnomAD v4: 21-17569730-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17569733_17569734dup , CM000683.2:g.17569733_17569734dup	GRCh38
NC_000021.8:g.18942051_18942052dup , CM000683.1:g.18942051_18942052dup	GRCh37
NC_000021.7:g.17863922_17863923dup	NCBI36
NG_029458.1:g.61828_61829dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000284878.12:c.*4041_*4042dup MANE Select	ENSP00000284878.7:n.*4041_*4042dup
ENST00000284878.11:c.*4041_*4042dup	ENSP00000284878.7:n.*4041_*4042dup
ENST00000400169.1:c.1017+4122_1017+4123dup	ENSP00000383033.1:n.1017+4122_1017+4123du...
NM_001207063.1:c.*4118_*4119dup	NP_001193992.1:n.*4118_*4119dup
NM_001207064.1:c.*4118_*4119dup	NP_001193993.1:n.*4118_*4119dup
NM_001207065.1:c.*4246_*4247dup	NP_001193994.1:n.*4246_*4247dup
NM_001207066.1:c.1017+4122_1017+4123dup	NP_001193995.1:n.1017+4122_1017+4123dup
NM_001338.4:c.*4041_*4042dup	NP_001329.1:n.*4041_*4042dup
XM_011529475.1:c.1017+4122_1017+4123dup	XP_011527777.1:n.1017+4122_1017+4123dup
XM_011529476.1:c.1017+4122_1017+4123dup	XP_011527778.1:n.1017+4122_1017+4123dup
XM_011529477.1:c.755+4122_755+4123dup	XP_011527779.1:n.755+4122_755+4123dup
XM_011529478.1:c.755+4122_755+4123dup	XP_011527780.1:n.755+4122_755+4123dup
XM_011529479.1:c.755+4122_755+4123dup	XP_011527781.1:n.755+4122_755+4123dup
XM_011529476.2:c.1017+4122_1017+4123dup	XP_011527778.1:n.1017+4122_1017+4123dup
XM_011529477.2:c.755+4122_755+4123dup	XP_011527779.1:n.755+4122_755+4123dup
XM_011529478.2:c.755+4122_755+4123dup	XP_011527780.1:n.755+4122_755+4123dup
XR_001754814.1:n.1131+4122_1131+4123dup
NM_001338.5:c.*4041_*4042dup MANE Select	NP_001329.1:n.*4041_*4042dup
NM_001207063.2:c.*4118_*4119dup	NP_001193992.1:n.*4118_*4119dup
NM_001207064.2:c.*4118_*4119dup	NP_001193993.1:n.*4118_*4119dup
NM_001207065.2:c.*4246_*4247dup	NP_001193994.1:n.*4246_*4247dup
NM_001207066.2:c.1017+4122_1017+4123dup	NP_001193995.1:n.1017+4122_1017+4123dup