Canonical Allele Identifier: CA347832127

Gene: CNGA3

Linked Data

• COSMIC: COSM331339
• MyVariant Identifiers: chr2:g.99012411G>T (hg19) ; chr2:g.98395948G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395948G>T , CM000664.2:g.98395948G>T	GRCh38
NC_000002.11:g.99012411G>T , CM000664.1:g.99012411G>T	GRCh37
NC_000002.10:g.98378843G>T	NCBI36
NG_009097.1:g.54794G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.778G>T MANE Select	ENSP00000272602.2:p.Asp260Tyr
ENST00000272602.6:c.778G>T	ENSP00000272602.2:p.Asp260Tyr
ENST00000393504.5:c.778G>T	ENSP00000377140.1:p.Asp260Tyr
ENST00000409937.1:c.790G>T	ENSP00000386761.1:p.Asp264Tyr
ENST00000436404.6:c.724G>T	ENSP00000410070.2:p.Asp242Tyr
NM_001079878.1:c.724G>T	NP_001073347.1:p.Asp242Tyr
NM_001298.2:c.778G>T	NP_001289.1:p.Asp260Tyr
XM_006712243.2:c.889G>T	XP_006712306.1:p.Asp297Tyr
XM_011510554.1:c.943G>T	XP_011508856.1:p.Asp315Tyr
XM_011510554.2:c.943G>T	XP_011508856.1:p.Asp315Tyr
NM_001079878.2:c.724G>T	NP_001073347.1:p.Asp242Tyr
NM_001298.3:c.778G>T MANE Select	NP_001289.1:p.Asp260Tyr