Canonical Allele Identifier: CA2654096292

Gene: CXADR

Linked Data

• gnomAD v4: 21-17569985-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17569986_17569987del , CM000683.2:g.17569986_17569987del	GRCh38
NC_000021.8:g.18942304_18942305del , CM000683.1:g.18942304_18942305del	GRCh37
NC_000021.7:g.17864175_17864176del	NCBI36
NG_029458.1:g.62081_62082del

Transcript Alleles

HGVS	Amino-acid change
ENST00000284878.12:c.*4294_*4295del MANE Select	ENSP00000284878.7:n.*4294_*4295del
ENST00000284878.11:c.*4294_*4295del	ENSP00000284878.7:n.*4294_*4295del
ENST00000400169.1:c.1017+4375_1017+4376del	ENSP00000383033.1:n.1017+4375_1017+4376de...
NM_001207063.1:c.*4371_*4372del	NP_001193992.1:n.*4371_*4372del
NM_001207064.1:c.*4371_*4372del	NP_001193993.1:n.*4371_*4372del
NM_001207065.1:c.*4499_*4500del	NP_001193994.1:n.*4499_*4500del
NM_001207066.1:c.1017+4375_1017+4376del	NP_001193995.1:n.1017+4375_1017+4376del
NM_001338.4:c.*4294_*4295del	NP_001329.1:n.*4294_*4295del
XM_011529475.1:c.1017+4375_1017+4376del	XP_011527777.1:n.1017+4375_1017+4376del
XM_011529476.1:c.1017+4375_1017+4376del	XP_011527778.1:n.1017+4375_1017+4376del
XM_011529477.1:c.755+4375_755+4376del	XP_011527779.1:n.755+4375_755+4376del
XM_011529478.1:c.755+4375_755+4376del	XP_011527780.1:n.755+4375_755+4376del
XM_011529479.1:c.755+4375_755+4376del	XP_011527781.1:n.755+4375_755+4376del
XM_011529476.2:c.1017+4375_1017+4376del	XP_011527778.1:n.1017+4375_1017+4376del
XM_011529477.2:c.755+4375_755+4376del	XP_011527779.1:n.755+4375_755+4376del
XM_011529478.2:c.755+4375_755+4376del	XP_011527780.1:n.755+4375_755+4376del
XR_001754814.1:n.1131+4375_1131+4376del
NM_001338.5:c.*4294_*4295del MANE Select	NP_001329.1:n.*4294_*4295del
NM_001207063.2:c.*4371_*4372del	NP_001193992.1:n.*4371_*4372del
NM_001207064.2:c.*4371_*4372del	NP_001193993.1:n.*4371_*4372del
NM_001207065.2:c.*4499_*4500del	NP_001193994.1:n.*4499_*4500del
NM_001207066.2:c.1017+4375_1017+4376del	NP_001193995.1:n.1017+4375_1017+4376del