Canonical Allele Identifier: CA2577489764

Gene: CXADR

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17570106G>A , CM000683.2:g.17570106G>A	GRCh38
NC_000021.8:g.18942424G>A , CM000683.1:g.18942424G>A	GRCh37
NC_000021.7:g.17864295G>A	NCBI36
NG_029458.1:g.62201G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400169.1:c.1017+4495G>A	ENSP00000383033.1:n.1017+4495G>A
NM_001207063.1:c.*4491G>A	NP_001193992.1:n.*4491G>A
NM_001207064.1:c.*4491G>A	NP_001193993.1:n.*4491G>A
NM_001207065.1:c.*4619G>A	NP_001193994.1:n.*4619G>A
NM_001207066.1:c.1017+4495G>A	NP_001193995.1:n.1017+4495G>A
NM_001338.4:c.*4414G>A	NP_001329.1:n.*4414G>A
XM_011529475.1:c.1017+4495G>A	XP_011527777.1:n.1017+4495G>A
XM_011529476.1:c.1017+4495G>A	XP_011527778.1:n.1017+4495G>A
XM_011529477.1:c.755+4495G>A	XP_011527779.1:n.755+4495G>A
XM_011529478.1:c.755+4495G>A	XP_011527780.1:n.755+4495G>A
XM_011529479.1:c.755+4495G>A	XP_011527781.1:n.755+4495G>A
XM_011529476.2:c.1017+4495G>A	XP_011527778.1:n.1017+4495G>A
XM_011529477.2:c.755+4495G>A	XP_011527779.1:n.755+4495G>A
XM_011529478.2:c.755+4495G>A	XP_011527780.1:n.755+4495G>A
XR_001754814.1:n.1131+4495G>A
NM_001207066.2:c.1017+4495G>A	NP_001193995.1:n.1017+4495G>A