Canonical Allele Identifier: CA177234589

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54621582G>A , CM000670.2:g.54621582G>A	GRCh38
NC_000008.10:g.55534142G>A , CM000670.1:g.55534142G>A	GRCh37
NC_000008.9:g.55696695G>A	NCBI36
NG_009840.1:g.10516G>A
NG_009840.2:g.10516G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006269.2:c.615+1G>A MANE Select	NP_006260.1:n.615+1G>A
ENST00000220676.2:c.615+1G>A MANE Select	ENSP00000220676.1:n.615+1G>A
NM_001375654.1:c.615+1G>A	NP_001362583.1:n.615+1G>A
NM_006269.1:c.615+1G>A	NP_006260.1:n.615+1G>A
ENST00000220676.1:c.615+1G>A	ENSP00000220676.1:n.615+1G>A
ENST00000636932.1:c.615+1G>A	ENSP00000489857.1:n.615+1G>A
ENST00000637698.1:c.615+1G>A	ENSP00000490104.1:n.615+1G>A
XM_017013721.1:c.636+1G>A	XP_016869210.1:n.636+1G>A
XM_017013722.1:c.615+1G>A	XP_016869211.1:n.615+1G>A