Canonical Allele Identifier: CA2654096239

Gene: CXADR

Linked Data

• gnomAD v4: 21-17569804-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17569804C>G , CM000683.2:g.17569804C>G	GRCh38
NC_000021.8:g.18942122C>G , CM000683.1:g.18942122C>G	GRCh37
NC_000021.7:g.17863993C>G	NCBI36
NG_029458.1:g.61899C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284878.12:c.*4112C>G MANE Select	ENSP00000284878.7:n.*4112C>G
ENST00000284878.11:c.*4112C>G	ENSP00000284878.7:n.*4112C>G
ENST00000400169.1:c.1017+4193C>G	ENSP00000383033.1:n.1017+4193C>G
NM_001207063.1:c.*4189C>G	NP_001193992.1:n.*4189C>G
NM_001207064.1:c.*4189C>G	NP_001193993.1:n.*4189C>G
NM_001207065.1:c.*4317C>G	NP_001193994.1:n.*4317C>G
NM_001207066.1:c.1017+4193C>G	NP_001193995.1:n.1017+4193C>G
NM_001338.4:c.*4112C>G	NP_001329.1:n.*4112C>G
XM_011529475.1:c.1017+4193C>G	XP_011527777.1:n.1017+4193C>G
XM_011529476.1:c.1017+4193C>G	XP_011527778.1:n.1017+4193C>G
XM_011529477.1:c.755+4193C>G	XP_011527779.1:n.755+4193C>G
XM_011529478.1:c.755+4193C>G	XP_011527780.1:n.755+4193C>G
XM_011529479.1:c.755+4193C>G	XP_011527781.1:n.755+4193C>G
XM_011529476.2:c.1017+4193C>G	XP_011527778.1:n.1017+4193C>G
XM_011529477.2:c.755+4193C>G	XP_011527779.1:n.755+4193C>G
XM_011529478.2:c.755+4193C>G	XP_011527780.1:n.755+4193C>G
XR_001754814.1:n.1131+4193C>G
NM_001338.5:c.*4112C>G MANE Select	NP_001329.1:n.*4112C>G
NM_001207063.2:c.*4189C>G	NP_001193992.1:n.*4189C>G
NM_001207064.2:c.*4189C>G	NP_001193993.1:n.*4189C>G
NM_001207065.2:c.*4317C>G	NP_001193994.1:n.*4317C>G
NM_001207066.2:c.1017+4193C>G	NP_001193995.1:n.1017+4193C>G