Canonical Allele Identifier: CA461100137

Gene: RP1

Linked Data

• MyVariant Identifiers: chr8:g.55540768A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54628208A>T , CM000670.2:g.54628208A>T	GRCh38
NC_000008.10:g.55540768A>T , CM000670.1:g.55540768A>T	GRCh37
NC_000008.9:g.55703321A>T	NCBI36
NG_009840.1:g.17142A>T
NG_009840.2:g.17142A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.4326A>T MANE Select	ENSP00000220676.1:p.Pro1442=
ENST00000636932.1:c.787+5920A>T	ENSP00000489857.1:n.787+5920A>T
ENST00000637698.1:c.787+5920A>T	ENSP00000490104.1:n.787+5920A>T
ENST00000220676.1:c.4326A>T	ENSP00000220676.1:p.Pro1442=
NM_006269.1:c.4326A>T	NP_006260.1:p.Pro1442=
XM_017013721.1:c.4347A>T	XP_016869210.1:p.Pro1449=
XM_017013722.1:c.4326A>T	XP_016869211.1:p.Pro1442=
NM_001375654.1:c.787+5920A>T	NP_001362583.1:n.787+5920A>T
NM_006269.2:c.4326A>T MANE Select	NP_006260.1:p.Pro1442=