Canonical Allele Identifier: CA2751373825

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98393809_98393811del , CM000664.2:g.98393809_98393811del	GRCh38
NC_000002.11:g.99010272_99010274del , CM000664.1:g.99010272_99010274del	GRCh37
NC_000002.10:g.98376704_98376706del	NCBI36
NG_009097.1:g.52655_52657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.673+1839_673+1841del MANE Select	ENSP00000272602.2:n.673+1839_673+1841del
ENST00000272602.6:c.673+1839_673+1841del	ENSP00000272602.2:n.673+1839_673+1841del
ENST00000393504.5:c.673+1839_673+1841del	ENSP00000377140.1:n.673+1839_673+1841del
ENST00000409937.1:c.685+1839_685+1841del	ENSP00000386761.1:n.685+1839_685+1841del
ENST00000436404.6:c.619+1839_619+1841del	ENSP00000410070.2:n.619+1839_619+1841del
NM_001079878.1:c.619+1839_619+1841del	NP_001073347.1:n.619+1839_619+1841del
NM_001298.2:c.673+1839_673+1841del	NP_001289.1:n.673+1839_673+1841del
XM_006712243.2:c.784+1839_784+1841del	XP_006712306.1:n.784+1839_784+1841del
XM_011510554.1:c.838+1839_838+1841del	XP_011508856.1:n.838+1839_838+1841del
XM_011510554.2:c.838+1839_838+1841del	XP_011508856.1:n.838+1839_838+1841del
NM_001079878.2:c.619+1839_619+1841del	NP_001073347.1:n.619+1839_619+1841del
NM_001298.3:c.673+1839_673+1841del MANE Select	NP_001289.1:n.673+1839_673+1841del