Canonical Allele Identifier: CA1159576977
Gene: RSRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25243642G= , CM000663.2:g.25243642G= GRCh38
NC_000001.10:g.25570133G= , CM000663.1:g.25570133G= GRCh37
NC_000001.9:g.25442720G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243189.12:c.673-9C= MANE Select ENSP00000243189.7:n.673-9C=
ENST00000243189.11:c.673-9C= ENSP00000243189.7:n.673-9C=
ENST00000473314.6:c.*619C= ENSP00000457582.1:n.*619C=
ENST00000475766.2:n.224-9C=
ENST00000498238.1:n.2392C=
ENST00000564223.5:n.13C=
ENST00000565733.5:c.350-9C=
ENST00000566395.5:c.290-9C=
ENST00000568254.5:c.*574C= ENSP00000457195.1:n.*574C=
ENST00000569495.5:n.464C=
ENST00000570063.5:n.1310-9C=
NM_020317.3:c.673-9C= NP_064713.3:n.673-9C=
XM_011541797.1:c.673-9C= XP_011540099.1:n.673-9C=
XM_011541798.1:c.*36-9C= XP_011540100.1:n.*36-9C=
XR_241200.1:n.1577C=
XR_241201.1:n.995-9C=
XR_946709.1:n.2228C=
XR_946710.1:n.1919-9C=
XR_946711.1:n.1646-9C=
XR_946712.1:n.1806C=
XR_946713.1:n.1532C=
NM_001321772.1:c.673-9C= NP_001308701.1:n.673-9C=
NM_020317.4:c.673-9C= NP_064713.3:n.673-9C=
NR_135143.1:n.2457C=
NR_135144.1:n.1532C=
NR_135777.1:n.2432C=
NR_135778.1:n.1806C=
NR_135780.1:n.1919-9C=
NR_135781.1:n.1577C=
NR_135782.1:n.1268-9C=
NR_135783.1:n.995-9C=
NR_135784.1:n.2457C=
NR_135785.1:n.994-9C=
NR_135786.1:n.2457C=
NR_135787.1:n.2581C=
NR_135788.1:n.2523C=
NR_135789.1:n.3461C=
XR_946709.2:n.2194C=
NM_020317.5:c.673-9C= MANE Select NP_064713.3:n.673-9C=
NR_135784.2:n.2392C=
NR_135786.2:n.2392C=
NM_001321772.2:c.673-9C= NP_001308701.1:n.673-9C=
NR_135143.2:n.2392C=
NR_135144.2:n.1467C=
NR_135777.2:n.2432C=
NR_135778.2:n.1741C=
NR_135780.2:n.1854-9C=
NR_135781.2:n.1512C=
NR_135782.2:n.1203-9C=
NR_135783.2:n.930-9C=
NR_135785.2:n.929-9C=
NR_135787.2:n.2581C=
NR_135788.2:n.2523C=
NR_135789.2:n.3461C=