Canonical Allele Identifier: CA347831462

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99006143G>A (hg19) ; chr2:g.98389680G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389680G>A , CM000664.2:g.98389680G>A	GRCh38
NC_000002.11:g.99006143G>A , CM000664.1:g.99006143G>A	GRCh37
NC_000002.10:g.98372575G>A	NCBI36
NG_009097.1:g.48526G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.472G>A MANE Select	ENSP00000272602.2:p.Ala158Thr
ENST00000272602.6:c.472G>A	ENSP00000272602.2:p.Ala158Thr
ENST00000393503.2:n.477G>A
ENST00000393504.5:c.472G>A	ENSP00000377140.1:p.Ala158Thr
ENST00000409937.1:c.484G>A	ENSP00000386761.1:p.Ala162Thr
ENST00000436404.6:c.418G>A	ENSP00000410070.2:p.Ala140Thr
NM_001079878.1:c.418G>A	NP_001073347.1:p.Ala140Thr
NM_001298.2:c.472G>A	NP_001289.1:p.Ala158Thr
XM_006712243.2:c.583G>A	XP_006712306.1:p.Ala195Thr
XM_011510554.1:c.637G>A	XP_011508856.1:p.Ala213Thr
XM_011510554.2:c.637G>A	XP_011508856.1:p.Ala213Thr
NM_001079878.2:c.418G>A	NP_001073347.1:p.Ala140Thr
NM_001298.3:c.472G>A MANE Select	NP_001289.1:p.Ala158Thr