Canonical Allele Identifier: CA318088719

Gene: CXADR

Linked Data

• dbSNP Id: rs993368566
• gnomAD v3: 21-17569963-A-T
• gnomAD v4: 21-17569963-A-T
• MyVariant Identifiers: chr21:g.18942281A>T (hg19) ; chr21:g.17569963A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17569963A>T , CM000683.2:g.17569963A>T	GRCh38
NC_000021.8:g.18942281A>T , CM000683.1:g.18942281A>T	GRCh37
NC_000021.7:g.17864152A>T	NCBI36
NG_029458.1:g.62058A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000284878.12:c.*4271A>T MANE Select	ENSP00000284878.7:n.*4271A>T
ENST00000284878.11:c.*4271A>T	ENSP00000284878.7:n.*4271A>T
ENST00000400169.1:c.1017+4352A>T	ENSP00000383033.1:n.1017+4352A>T
NM_001207063.1:c.*4348A>T	NP_001193992.1:n.*4348A>T
NM_001207064.1:c.*4348A>T	NP_001193993.1:n.*4348A>T
NM_001207065.1:c.*4476A>T	NP_001193994.1:n.*4476A>T
NM_001207066.1:c.1017+4352A>T	NP_001193995.1:n.1017+4352A>T
NM_001338.4:c.*4271A>T	NP_001329.1:n.*4271A>T
XM_011529475.1:c.1017+4352A>T	XP_011527777.1:n.1017+4352A>T
XM_011529476.1:c.1017+4352A>T	XP_011527778.1:n.1017+4352A>T
XM_011529477.1:c.755+4352A>T	XP_011527779.1:n.755+4352A>T
XM_011529478.1:c.755+4352A>T	XP_011527780.1:n.755+4352A>T
XM_011529479.1:c.755+4352A>T	XP_011527781.1:n.755+4352A>T
XM_011529476.2:c.1017+4352A>T	XP_011527778.1:n.1017+4352A>T
XM_011529477.2:c.755+4352A>T	XP_011527779.1:n.755+4352A>T
XM_011529478.2:c.755+4352A>T	XP_011527780.1:n.755+4352A>T
XR_001754814.1:n.1131+4352A>T
NM_001338.5:c.*4271A>T MANE Select	NP_001329.1:n.*4271A>T
NM_001207063.2:c.*4348A>T	NP_001193992.1:n.*4348A>T
NM_001207064.2:c.*4348A>T	NP_001193993.1:n.*4348A>T
NM_001207065.2:c.*4476A>T	NP_001193994.1:n.*4476A>T
NM_001207066.2:c.1017+4352A>T	NP_001193995.1:n.1017+4352A>T