Canonical Allele Identifier: CA1273419724
Gene: CNGA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98396017C= , CM000664.2:g.98396017C= GRCh38
NC_000002.11:g.99012480C= , CM000664.1:g.99012480C= GRCh37
NC_000002.10:g.98378912C= NCBI36
NG_009097.1:g.54863C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272602.7:c.847C= MANE Select ENSP00000272602.2:p.Arg283=
ENST00000272602.6:c.847C= ENSP00000272602.2:p.Arg283=
ENST00000393504.5:c.847C= ENSP00000377140.1:p.Arg283=
ENST00000409937.1:c.859C= ENSP00000386761.1:p.Arg287=
ENST00000436404.6:c.793C= ENSP00000410070.2:p.Arg265=
NM_001079878.1:c.793C= NP_001073347.1:p.Arg265=
NM_001298.2:c.847C= NP_001289.1:p.Arg283=
XM_006712243.2:c.958C= XP_006712306.1:p.Arg320=
XM_011510554.1:c.1012C= XP_011508856.1:p.Arg338=
XM_011510554.2:c.1012C= XP_011508856.1:p.Arg338=
NM_001079878.2:c.793C= NP_001073347.1:p.Arg265=
NM_001298.3:c.847C= MANE Select NP_001289.1:p.Arg283=