Canonical Allele Identifier: CA2379412210

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17569968G= , CM000683.2:g.17569968G=	GRCh38
NC_000021.8:g.18942286G= , CM000683.1:g.18942286G=	GRCh37
NC_000021.7:g.17864157G=	NCBI36
NG_029458.1:g.62063G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000284878.12:c.*4276G= MANE Select	ENSP00000284878.7:n.*4276G=
ENST00000284878.11:c.*4276G=	ENSP00000284878.7:n.*4276G=
ENST00000400169.1:c.1017+4357G=	ENSP00000383033.1:n.1017+4357G=
NM_001207063.1:c.*4353G=	NP_001193992.1:n.*4353G=
NM_001207064.1:c.*4353G=	NP_001193993.1:n.*4353G=
NM_001207065.1:c.*4481G=	NP_001193994.1:n.*4481G=
NM_001207066.1:c.1017+4357G=	NP_001193995.1:n.1017+4357G=
NM_001338.4:c.*4276G=	NP_001329.1:n.*4276G=
XM_011529475.1:c.1017+4357G=	XP_011527777.1:n.1017+4357G=
XM_011529476.1:c.1017+4357G=	XP_011527778.1:n.1017+4357G=
XM_011529477.1:c.755+4357G=	XP_011527779.1:n.755+4357G=
XM_011529478.1:c.755+4357G=	XP_011527780.1:n.755+4357G=
XM_011529479.1:c.755+4357G=	XP_011527781.1:n.755+4357G=
XM_011529476.2:c.1017+4357G=	XP_011527778.1:n.1017+4357G=
XM_011529477.2:c.755+4357G=	XP_011527779.1:n.755+4357G=
XM_011529478.2:c.755+4357G=	XP_011527780.1:n.755+4357G=
XR_001754814.1:n.1131+4357G=
NM_001338.5:c.*4276G= MANE Select	NP_001329.1:n.*4276G=
NM_001207063.2:c.*4353G=	NP_001193992.1:n.*4353G=
NM_001207064.2:c.*4353G=	NP_001193993.1:n.*4353G=
NM_001207065.2:c.*4481G=	NP_001193994.1:n.*4481G=
NM_001207066.2:c.1017+4357G=	NP_001193995.1:n.1017+4357G=