Canonical Allele Identifier: CA1273420048
Gene: CNGA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98396749C= , CM000664.2:g.98396749C= GRCh38
NC_000002.11:g.99013212C= , CM000664.1:g.99013212C= GRCh37
NC_000002.10:g.98379644C= NCBI36
NG_009097.1:g.55595C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272602.7:c.1579C= MANE Select ENSP00000272602.2:p.Leu527=
ENST00000272602.6:c.1579C= ENSP00000272602.2:p.Leu527=
ENST00000393504.5:c.1579C= ENSP00000377140.1:p.Leu527=
ENST00000409937.1:c.1591C= ENSP00000386761.1:p.Leu531=
ENST00000436404.6:c.1525C= ENSP00000410070.2:p.Leu509=
NM_001079878.1:c.1525C= NP_001073347.1:p.Leu509=
NM_001298.2:c.1579C= NP_001289.1:p.Leu527=
XM_006712243.2:c.1690C= XP_006712306.1:p.Leu564=
XM_011510554.1:c.1744C= XP_011508856.1:p.Leu582=
XM_011510554.2:c.1744C= XP_011508856.1:p.Leu582=
NM_001079878.2:c.1525C= NP_001073347.1:p.Leu509=
NM_001298.3:c.1579C= MANE Select NP_001289.1:p.Leu527=