Canonical Allele Identifier: CA1273420047
Gene: CNGA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98396748G= , CM000664.2:g.98396748G= GRCh38
NC_000002.11:g.99013211G= , CM000664.1:g.99013211G= GRCh37
NC_000002.10:g.98379643G= NCBI36
NG_009097.1:g.55594G=

Transcript Alleles

HGVS Amino-acid change
ENST00000272602.7:c.1578G= MANE Select ENSP00000272602.2:p.Lys526=
ENST00000272602.6:c.1578G= ENSP00000272602.2:p.Lys526=
ENST00000393504.5:c.1578G= ENSP00000377140.1:p.Lys526=
ENST00000409937.1:c.1590G= ENSP00000386761.1:p.Lys530=
ENST00000436404.6:c.1524G= ENSP00000410070.2:p.Lys508=
NM_001079878.1:c.1524G= NP_001073347.1:p.Lys508=
NM_001298.2:c.1578G= NP_001289.1:p.Lys526=
XM_006712243.2:c.1689G= XP_006712306.1:p.Lys563=
XM_011510554.1:c.1743G= XP_011508856.1:p.Lys581=
XM_011510554.2:c.1743G= XP_011508856.1:p.Lys581=
NM_001079878.2:c.1524G= NP_001073347.1:p.Lys508=
NM_001298.3:c.1578G= MANE Select NP_001289.1:p.Lys526=