Canonical Allele Identifier: CA347832023
Gene: CNGA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98395898A>T , CM000664.2:g.98395898A>T GRCh38
NC_000002.11:g.99012361A>T , CM000664.1:g.99012361A>T GRCh37
NC_000002.10:g.98378793A>T NCBI36
NG_009097.1:g.54744A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272602.7:c.728A>T MANE Select ENSP00000272602.2:p.Tyr243Phe
ENST00000272602.6:c.728A>T ENSP00000272602.2:p.Tyr243Phe
ENST00000393504.5:c.728A>T ENSP00000377140.1:p.Tyr243Phe
ENST00000409937.1:c.740A>T ENSP00000386761.1:p.Tyr247Phe
ENST00000436404.6:c.674A>T ENSP00000410070.2:p.Tyr225Phe
NM_001079878.1:c.674A>T NP_001073347.1:p.Tyr225Phe
NM_001298.2:c.728A>T NP_001289.1:p.Tyr243Phe
XM_006712243.2:c.839A>T XP_006712306.1:p.Tyr280Phe
XM_011510554.1:c.893A>T XP_011508856.1:p.Tyr298Phe
XM_011510554.2:c.893A>T XP_011508856.1:p.Tyr298Phe
NM_001079878.2:c.674A>T NP_001073347.1:p.Tyr225Phe
NM_001298.3:c.728A>T MANE Select NP_001289.1:p.Tyr243Phe