Canonical Allele Identifier: CA347832125

Gene: CNGA3

Linked Data

• gnomAD v4: 2-98395946-C-G
• MyVariant Identifiers: chr2:g.99012409C>G (hg19) ; chr2:g.98395946C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395946C>G , CM000664.2:g.98395946C>G	GRCh38
NC_000002.11:g.99012409C>G , CM000664.1:g.99012409C>G	GRCh37
NC_000002.10:g.98378841C>G	NCBI36
NG_009097.1:g.54792C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.776C>G MANE Select	ENSP00000272602.2:p.Thr259Ser
ENST00000272602.6:c.776C>G	ENSP00000272602.2:p.Thr259Ser
ENST00000393504.5:c.776C>G	ENSP00000377140.1:p.Thr259Ser
ENST00000409937.1:c.788C>G	ENSP00000386761.1:p.Thr263Ser
ENST00000436404.6:c.722C>G	ENSP00000410070.2:p.Thr241Ser
NM_001079878.1:c.722C>G	NP_001073347.1:p.Thr241Ser
NM_001298.2:c.776C>G	NP_001289.1:p.Thr259Ser
XM_006712243.2:c.887C>G	XP_006712306.1:p.Thr296Ser
XM_011510554.1:c.941C>G	XP_011508856.1:p.Thr314Ser
XM_011510554.2:c.941C>G	XP_011508856.1:p.Thr314Ser
NM_001079878.2:c.722C>G	NP_001073347.1:p.Thr241Ser
NM_001298.3:c.776C>G MANE Select	NP_001289.1:p.Thr259Ser