Canonical Allele Identifier: CA2911255

Gene: CNGA1 NIPAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47942030A>G , CM000666.2:g.47942030A>G	GRCh38
NC_000004.11:g.47944047A>G , CM000666.1:g.47944047A>G	GRCh37
NC_000004.10:g.47638804A>G	NCBI36
NG_009193.1:g.75915T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001379270.1:c.545+11T>C (CNGA1) MANE Select	NP_001366199.1:n.545+11T>C
ENST00000514170.7:c.545+11T>C (CNGA1) MANE Select	ENSP00000426862.3:n.545+11T>C
NM_000087.3:c.557+11T>C (CNGA1)	NP_000078.2:n.557+11T>C
NM_000087.4:c.557+11T>C (CNGA1)	NP_000078.2:n.557+11T>C
NM_000087.5:c.545+11T>C (CNGA1)	NP_000078.3:n.545+11T>C
NM_001142564.1:c.764+11T>C (CNGA1)	NP_001136036.1:n.764+11T>C
NM_001142564.2:c.545+11T>C (CNGA1)	NP_001136036.2:n.545+11T>C
NM_001375386.1:c.557+11T>C (CNGA1)	NP_001362315.1:n.557+11T>C
NR_125879.1:n.479-16994A>G
ENST00000358519.8:c.557+11T>C (CNGA1)	ENSP00000351320.4:n.557+11T>C
ENST00000402813.7:c.764+11T>C (CNGA1)	ENSP00000384264.3:n.764+11T>C
ENST00000402813.9:c.545+11T>C (CNGA1)	ENSP00000384264.5:n.545+11T>C
ENST00000420489.6:c.557+11T>C (CNGA1)	ENSP00000389881.2:n.557+11T>C
ENST00000420489.7:c.545+11T>C (CNGA1)	ENSP00000389881.3:n.545+11T>C
ENST00000500571.2:n.479-16994A>G (NIPAL1)
ENST00000513724.1:n.563+27326A>G (NIPAL1)
ENST00000514170.5:c.557+11T>C (CNGA1)	ENSP00000426862.1:n.557+11T>C
ENST00000544810.5:c.764+11T>C (CNGA1)	ENSP00000443401.2:n.764+11T>C
XM_005248049.3:c.557+11T>C (CNGA1)	XP_005248106.1:n.557+11T>C
XM_005248049.4:c.782+11T>C (CNGA1)	XP_005248106.2:n.782+11T>C
XM_011513623.1:c.557+11T>C (CNGA1)	XP_011511925.1:n.557+11T>C
XM_011513623.2:c.557+11T>C (CNGA1)	XP_011511925.1:n.557+11T>C
XM_017007712.1:c.557+11T>C (CNGA1)	XP_016863201.1:n.557+11T>C