Canonical Allele Identifier: CA2379412251

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17570057T= , CM000683.2:g.17570057T=	GRCh38
NC_000021.8:g.18942375T= , CM000683.1:g.18942375T=	GRCh37
NC_000021.7:g.17864246T=	NCBI36
NG_029458.1:g.62152T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284878.12:c.*4365T= MANE Select	ENSP00000284878.7:n.*4365T=
ENST00000284878.11:c.*4365T=	ENSP00000284878.7:n.*4365T=
ENST00000400169.1:c.1017+4446T=	ENSP00000383033.1:n.1017+4446T=
NM_001207063.1:c.*4442T=	NP_001193992.1:n.*4442T=
NM_001207064.1:c.*4442T=	NP_001193993.1:n.*4442T=
NM_001207065.1:c.*4570T=	NP_001193994.1:n.*4570T=
NM_001207066.1:c.1017+4446T=	NP_001193995.1:n.1017+4446T=
NM_001338.4:c.*4365T=	NP_001329.1:n.*4365T=
XM_011529475.1:c.1017+4446T=	XP_011527777.1:n.1017+4446T=
XM_011529476.1:c.1017+4446T=	XP_011527778.1:n.1017+4446T=
XM_011529477.1:c.755+4446T=	XP_011527779.1:n.755+4446T=
XM_011529478.1:c.755+4446T=	XP_011527780.1:n.755+4446T=
XM_011529479.1:c.755+4446T=	XP_011527781.1:n.755+4446T=
XM_011529476.2:c.1017+4446T=	XP_011527778.1:n.1017+4446T=
XM_011529477.2:c.755+4446T=	XP_011527779.1:n.755+4446T=
XM_011529478.2:c.755+4446T=	XP_011527780.1:n.755+4446T=
XR_001754814.1:n.1131+4446T=
NM_001338.5:c.*4365T= MANE Select	NP_001329.1:n.*4365T=
NM_001207063.2:c.*4442T=	NP_001193992.1:n.*4442T=
NM_001207064.2:c.*4442T=	NP_001193993.1:n.*4442T=
NM_001207065.2:c.*4570T=	NP_001193994.1:n.*4570T=
NM_001207066.2:c.1017+4446T=	NP_001193995.1:n.1017+4446T=