Canonical Allele Identifier: CA356823336

Gene: CNGA1 NIPAL1

Linked Data

• ClinVar Variation Id: 1910171
• ClinVar RCV Id: RCV002593069
• dbSNP Id: rs373782782
• gnomAD v2: 4-47938625-C-A
• gnomAD v4: 4-47936608-C-A
• MyVariant Identifiers: chr4:g.47938625C>A (hg19) ; chr4:g.47936608C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47936608C>A , CM000666.2:g.47936608C>A	GRCh38
NC_000004.11:g.47938625C>A , CM000666.1:g.47938625C>A	GRCh37
NC_000004.10:g.47633382C>A	NCBI36
NG_009193.1:g.81337G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402813.9:c.1874G>T (CNGA1)	ENSP00000384264.5:p.Arg625Leu
ENST00000420489.7:c.1874G>T (CNGA1)	ENSP00000389881.3:p.Arg625Leu
ENST00000514170.7:c.1874G>T (CNGA1) MANE Select	ENSP00000426862.3:p.Arg625Leu
ENST00000358519.8:c.1886G>T (CNGA1)	ENSP00000351320.4:p.Arg629Leu
ENST00000402813.7:c.2093G>T (CNGA1)	ENSP00000384264.3:p.Arg698Leu
ENST00000420489.6:c.1886G>T (CNGA1)	ENSP00000389881.2:p.Arg629Leu
ENST00000500571.2:n.478+21904C>A (NIPAL1)
ENST00000513724.1:n.563+21904C>A (NIPAL1)
ENST00000514170.5:c.1886G>T (CNGA1)	ENSP00000426862.1:p.Arg629Leu
ENST00000544810.5:c.2093G>T (CNGA1)	ENSP00000443401.2:p.Arg698Leu
NM_000087.3:c.1886G>T (CNGA1)	NP_000078.2:p.Arg629Leu
NM_001142564.1:c.2093G>T (CNGA1)	NP_001136036.1:p.Arg698Leu
NR_125879.1:n.478+21904C>A
XM_005248049.3:c.1886G>T (CNGA1)	XP_005248106.1:p.Arg629Leu
XM_011513623.1:c.1886G>T (CNGA1)	XP_011511925.1:p.Arg629Leu
XM_005248049.4:c.2111G>T (CNGA1)	XP_005248106.2:p.Arg704Leu
XM_011513623.2:c.1886G>T (CNGA1)	XP_011511925.1:p.Arg629Leu
XM_017007712.1:c.1886G>T (CNGA1)	XP_016863201.1:p.Arg629Leu
NM_000087.4:c.1886G>T (CNGA1)	NP_000078.2:p.Arg629Leu
NM_001375386.1:c.1886G>T (CNGA1)	NP_001362315.1:p.Arg629Leu
NM_000087.5:c.1874G>T (CNGA1)	NP_000078.3:p.Arg625Leu
NM_001142564.2:c.1874G>T (CNGA1)	NP_001136036.2:p.Arg625Leu
NM_001379270.1:c.1874G>T (CNGA1) MANE Select	NP_001366199.1:p.Arg625Leu