Canonical Allele Identifier: CA347832002
Gene: CNGA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98395890G>C , CM000664.2:g.98395890G>C GRCh38
NC_000002.11:g.99012353G>C , CM000664.1:g.99012353G>C GRCh37
NC_000002.10:g.98378785G>C NCBI36
NG_009097.1:g.54736G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272602.7:c.720G>C MANE Select ENSP00000272602.2:p.Trp240Cys
ENST00000272602.6:c.720G>C ENSP00000272602.2:p.Trp240Cys
ENST00000393504.5:c.720G>C ENSP00000377140.1:p.Trp240Cys
ENST00000409937.1:c.732G>C ENSP00000386761.1:p.Trp244Cys
ENST00000436404.6:c.666G>C ENSP00000410070.2:p.Trp222Cys
NM_001079878.1:c.666G>C NP_001073347.1:p.Trp222Cys
NM_001298.2:c.720G>C NP_001289.1:p.Trp240Cys
XM_006712243.2:c.831G>C XP_006712306.1:p.Trp277Cys
XM_011510554.1:c.885G>C XP_011508856.1:p.Trp295Cys
XM_011510554.2:c.885G>C XP_011508856.1:p.Trp295Cys
NM_001079878.2:c.666G>C NP_001073347.1:p.Trp222Cys
NM_001298.3:c.720G>C MANE Select NP_001289.1:p.Trp240Cys