Canonical Allele Identifier: CA1144150350
Gene: RSRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25243678G= , CM000663.2:g.25243678G= GRCh38
NC_000001.10:g.25570169G= , CM000663.1:g.25570169G= GRCh37
NC_000001.9:g.25442756G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243189.12:c.673-45C= MANE Select ENSP00000243189.7:n.673-45C=
ENST00000243189.11:c.673-45C= ENSP00000243189.7:n.673-45C=
ENST00000473314.6:c.*583C= ENSP00000457582.1:n.*583C=
ENST00000475766.2:n.224-45C=
ENST00000498238.1:n.2356C=
ENST00000565733.5:c.350-45C=
ENST00000566395.5:c.290-45C=
ENST00000568254.5:c.*538C= ENSP00000457195.1:n.*538C=
ENST00000569495.5:n.428C=
ENST00000570063.5:n.1310-45C=
NM_020317.3:c.673-45C= NP_064713.3:n.673-45C=
XM_011541797.1:c.673-45C= XP_011540099.1:n.673-45C=
XM_011541798.1:c.*36-45C= XP_011540100.1:n.*36-45C=
XR_241200.1:n.1541C=
XR_241201.1:n.995-45C=
XR_946709.1:n.2192C=
XR_946710.1:n.1919-45C=
XR_946711.1:n.1646-45C=
XR_946712.1:n.1770C=
XR_946713.1:n.1496C=
NM_001321772.1:c.673-45C= NP_001308701.1:n.673-45C=
NM_020317.4:c.673-45C= NP_064713.3:n.673-45C=
NR_135143.1:n.2421C=
NR_135144.1:n.1496C=
NR_135777.1:n.2396C=
NR_135778.1:n.1770C=
NR_135780.1:n.1919-45C=
NR_135781.1:n.1541C=
NR_135782.1:n.1268-45C=
NR_135783.1:n.995-45C=
NR_135784.1:n.2421C=
NR_135785.1:n.994-45C=
NR_135786.1:n.2421C=
NR_135787.1:n.2545C=
NR_135788.1:n.2487C=
NR_135789.1:n.3425C=
XR_946709.2:n.2158C=
NM_020317.5:c.673-45C= MANE Select NP_064713.3:n.673-45C=
NR_135784.2:n.2356C=
NR_135786.2:n.2356C=
NM_001321772.2:c.673-45C= NP_001308701.1:n.673-45C=
NR_135143.2:n.2356C=
NR_135144.2:n.1431C=
NR_135777.2:n.2396C=
NR_135778.2:n.1705C=
NR_135780.2:n.1854-45C=
NR_135781.2:n.1476C=
NR_135782.2:n.1203-45C=
NR_135783.2:n.930-45C=
NR_135785.2:n.929-45C=
NR_135787.2:n.2545C=
NR_135788.2:n.2487C=
NR_135789.2:n.3425C=