Canonical Allele Identifier: CA347832000
Gene: CNGA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98395889G>T , CM000664.2:g.98395889G>T GRCh38
NC_000002.11:g.99012352G>T , CM000664.1:g.99012352G>T GRCh37
NC_000002.10:g.98378784G>T NCBI36
NG_009097.1:g.54735G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272602.7:c.719G>T MANE Select ENSP00000272602.2:p.Trp240Leu
ENST00000272602.6:c.719G>T ENSP00000272602.2:p.Trp240Leu
ENST00000393504.5:c.719G>T ENSP00000377140.1:p.Trp240Leu
ENST00000409937.1:c.731G>T ENSP00000386761.1:p.Trp244Leu
ENST00000436404.6:c.665G>T ENSP00000410070.2:p.Trp222Leu
NM_001079878.1:c.665G>T NP_001073347.1:p.Trp222Leu
NM_001298.2:c.719G>T NP_001289.1:p.Trp240Leu
XM_006712243.2:c.830G>T XP_006712306.1:p.Trp277Leu
XM_011510554.1:c.884G>T XP_011508856.1:p.Trp295Leu
XM_011510554.2:c.884G>T XP_011508856.1:p.Trp295Leu
NM_001079878.2:c.665G>T NP_001073347.1:p.Trp222Leu
NM_001298.3:c.719G>T MANE Select NP_001289.1:p.Trp240Leu