Canonical Allele Identifier: CA370994016

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54626397C>T , CM000670.2:g.54626397C>T	GRCh38
NC_000008.10:g.55538957C>T , CM000670.1:g.55538957C>T	GRCh37
NC_000008.9:g.55701510C>T	NCBI36
NG_009840.1:g.15331C>T
NG_009840.2:g.15331C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006269.2:c.2515C>T MANE Select	NP_006260.1:p.Gln839Ter
ENST00000220676.2:c.2515C>T MANE Select	ENSP00000220676.1:p.Gln839Ter
NM_001375654.1:c.787+4109C>T	NP_001362583.1:n.787+4109C>T
NM_006269.1:c.2515C>T	NP_006260.1:p.Gln839Ter
ENST00000220676.1:c.2515C>T	ENSP00000220676.1:p.Gln839Ter
ENST00000636932.1:c.787+4109C>T	ENSP00000489857.1:n.787+4109C>T
ENST00000637698.1:c.787+4109C>T	ENSP00000490104.1:n.787+4109C>T
XM_017013721.1:c.2536C>T	XP_016869210.1:p.Gln846Ter
XM_017013722.1:c.2515C>T	XP_016869211.1:p.Gln839Ter