Canonical Allele Identifier: CA535104034
Gene: CNGA3 HGNC NCBI

Linked Data

dbSNP Id: rs1349517446

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98395720_98395721dup , CM000664.2:g.98395720_98395721dup GRCh38
NC_000002.11:g.99012183_99012184dup , CM000664.1:g.99012183_99012184dup GRCh37
NC_000002.10:g.98378615_98378616dup NCBI36
NG_009097.1:g.54566_54567dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000272602.7:c.674-124_674-123dup MANE Select ENSP00000272602.2:n.674-124_674-123dup
ENST00000272602.6:c.674-124_674-123dup ENSP00000272602.2:n.674-124_674-123dup
ENST00000393504.5:c.674-124_674-123dup ENSP00000377140.1:n.674-124_674-123dup
ENST00000409937.1:c.686-124_686-123dup ENSP00000386761.1:n.686-124_686-123dup
ENST00000436404.6:c.620-124_620-123dup ENSP00000410070.2:n.620-124_620-123dup
NM_001079878.1:c.620-124_620-123dup NP_001073347.1:n.620-124_620-123dup
NM_001298.2:c.674-124_674-123dup NP_001289.1:n.674-124_674-123dup
XM_006712243.2:c.785-124_785-123dup XP_006712306.1:n.785-124_785-123dup
XM_011510554.1:c.839-124_839-123dup XP_011508856.1:n.839-124_839-123dup
XM_011510554.2:c.839-124_839-123dup XP_011508856.1:n.839-124_839-123dup
NM_001079878.2:c.620-124_620-123dup NP_001073347.1:n.620-124_620-123dup
NM_001298.3:c.674-124_674-123dup MANE Select NP_001289.1:n.674-124_674-123dup