Canonical Allele Identifier: CA2379412104

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17569702T= , CM000683.2:g.17569702T=	GRCh38
NC_000021.8:g.18942020T= , CM000683.1:g.18942020T=	GRCh37
NC_000021.7:g.17863891T=	NCBI36
NG_029458.1:g.61797T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284878.12:c.*4010T= MANE Select	ENSP00000284878.7:n.*4010T=
ENST00000284878.11:c.*4010T=	ENSP00000284878.7:n.*4010T=
ENST00000400169.1:c.1017+4091T=	ENSP00000383033.1:n.1017+4091T=
NM_001207063.1:c.*4087T=	NP_001193992.1:n.*4087T=
NM_001207064.1:c.*4087T=	NP_001193993.1:n.*4087T=
NM_001207065.1:c.*4215T=	NP_001193994.1:n.*4215T=
NM_001207066.1:c.1017+4091T=	NP_001193995.1:n.1017+4091T=
NM_001338.4:c.*4010T=	NP_001329.1:n.*4010T=
XM_011529475.1:c.1017+4091T=	XP_011527777.1:n.1017+4091T=
XM_011529476.1:c.1017+4091T=	XP_011527778.1:n.1017+4091T=
XM_011529477.1:c.755+4091T=	XP_011527779.1:n.755+4091T=
XM_011529478.1:c.755+4091T=	XP_011527780.1:n.755+4091T=
XM_011529479.1:c.755+4091T=	XP_011527781.1:n.755+4091T=
XM_011529476.2:c.1017+4091T=	XP_011527778.1:n.1017+4091T=
XM_011529477.2:c.755+4091T=	XP_011527779.1:n.755+4091T=
XM_011529478.2:c.755+4091T=	XP_011527780.1:n.755+4091T=
XR_001754814.1:n.1131+4091T=
NM_001338.5:c.*4010T= MANE Select	NP_001329.1:n.*4010T=
NM_001207063.2:c.*4087T=	NP_001193992.1:n.*4087T=
NM_001207064.2:c.*4087T=	NP_001193993.1:n.*4087T=
NM_001207065.2:c.*4215T=	NP_001193994.1:n.*4215T=
NM_001207066.2:c.1017+4091T=	NP_001193995.1:n.1017+4091T=