Canonical Allele Identifier: CA1785188194
Gene: RP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54626176C= , CM000670.2:g.54626176C= GRCh38
NC_000008.10:g.55538736C= , CM000670.1:g.55538736C= GRCh37
NC_000008.9:g.55701289C= NCBI36
NG_009840.1:g.15110C=
NG_009840.2:g.15110C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.2294C= MANE Select ENSP00000220676.1:p.Thr765=
ENST00000636932.1:c.787+3888C= ENSP00000489857.1:n.787+3888C=
ENST00000637698.1:c.787+3888C= ENSP00000490104.1:n.787+3888C=
ENST00000220676.1:c.2294C= ENSP00000220676.1:p.Thr765=
NM_006269.1:c.2294C= NP_006260.1:p.Thr765=
XM_017013721.1:c.2315C= XP_016869210.1:p.Thr772=
XM_017013722.1:c.2294C= XP_016869211.1:p.Thr765=
NM_001375654.1:c.787+3888C= NP_001362583.1:n.787+3888C=
NM_006269.2:c.2294C= MANE Select NP_006260.1:p.Thr765=