Canonical Allele Identifier: CA1273419691
Gene: CNGA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98395947C= , CM000664.2:g.98395947C= GRCh38
NC_000002.11:g.99012410C= , CM000664.1:g.99012410C= GRCh37
NC_000002.10:g.98378842C= NCBI36
NG_009097.1:g.54793C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272602.7:c.777C= MANE Select ENSP00000272602.2:p.Thr259=
ENST00000272602.6:c.777C= ENSP00000272602.2:p.Thr259=
ENST00000393504.5:c.777C= ENSP00000377140.1:p.Thr259=
ENST00000409937.1:c.789C= ENSP00000386761.1:p.Thr263=
ENST00000436404.6:c.723C= ENSP00000410070.2:p.Thr241=
NM_001079878.1:c.723C= NP_001073347.1:p.Thr241=
NM_001298.2:c.777C= NP_001289.1:p.Thr259=
XM_006712243.2:c.888C= XP_006712306.1:p.Thr296=
XM_011510554.1:c.942C= XP_011508856.1:p.Thr314=
XM_011510554.2:c.942C= XP_011508856.1:p.Thr314=
NM_001079878.2:c.723C= NP_001073347.1:p.Thr241=
NM_001298.3:c.777C= MANE Select NP_001289.1:p.Thr259=