Canonical Allele Identifier: CA1273418774
Gene: CNGA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98393961A= , CM000664.2:g.98393961A= GRCh38
NC_000002.11:g.99010424A= , CM000664.1:g.99010424A= GRCh37
NC_000002.10:g.98376856A= NCBI36
NG_009097.1:g.52807A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272602.7:c.674-1883A= MANE Select ENSP00000272602.2:n.674-1883A=
ENST00000272602.6:c.674-1883A= ENSP00000272602.2:n.674-1883A=
ENST00000393504.5:c.674-1883A= ENSP00000377140.1:n.674-1883A=
ENST00000409937.1:c.686-1883A= ENSP00000386761.1:n.686-1883A=
ENST00000436404.6:c.620-1883A= ENSP00000410070.2:n.620-1883A=
NM_001079878.1:c.620-1883A= NP_001073347.1:n.620-1883A=
NM_001298.2:c.674-1883A= NP_001289.1:n.674-1883A=
XM_006712243.2:c.785-1883A= XP_006712306.1:n.785-1883A=
XM_011510554.1:c.839-1883A= XP_011508856.1:n.839-1883A=
XM_011510554.2:c.839-1883A= XP_011508856.1:n.839-1883A=
NM_001079878.2:c.620-1883A= NP_001073347.1:n.620-1883A=
NM_001298.3:c.674-1883A= MANE Select NP_001289.1:n.674-1883A=