Canonical Allele Identifier: CA427568121

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99012350G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395887G>C , CM000664.2:g.98395887G>C	GRCh38
NC_000002.11:g.99012350G>C , CM000664.1:g.99012350G>C	GRCh37
NC_000002.10:g.98378782G>C	NCBI36
NG_009097.1:g.54733G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.717G>C MANE Select	ENSP00000272602.2:p.Leu239=
ENST00000272602.6:c.717G>C	ENSP00000272602.2:p.Leu239=
ENST00000393504.5:c.717G>C	ENSP00000377140.1:p.Leu239=
ENST00000409937.1:c.729G>C	ENSP00000386761.1:p.Leu243=
ENST00000436404.6:c.663G>C	ENSP00000410070.2:p.Leu221=
NM_001079878.1:c.663G>C	NP_001073347.1:p.Leu221=
NM_001298.2:c.717G>C	NP_001289.1:p.Leu239=
XM_006712243.2:c.828G>C	XP_006712306.1:p.Leu276=
XM_011510554.1:c.882G>C	XP_011508856.1:p.Leu294=
XM_011510554.2:c.882G>C	XP_011508856.1:p.Leu294=
NM_001079878.2:c.663G>C	NP_001073347.1:p.Leu221=
NM_001298.3:c.717G>C MANE Select	NP_001289.1:p.Leu239=