Canonical Allele Identifier: CA1159576965
Gene: RSRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25243602C= , CM000663.2:g.25243602C= GRCh38
NC_000001.10:g.25570093C= , CM000663.1:g.25570093C= GRCh37
NC_000001.9:g.25442680C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243189.12:c.704G= MANE Select ENSP00000243189.7:p.Arg235=
ENST00000243189.11:c.704G= ENSP00000243189.7:p.Arg235=
ENST00000473314.6:c.*659G= ENSP00000457582.1:n.*659G=
ENST00000475766.2:n.255G=
ENST00000498238.1:n.2432G=
ENST00000564223.5:n.53G=
ENST00000565733.5:c.381G=
ENST00000566395.5:c.321G=
ENST00000568254.5:c.*614G= ENSP00000457195.1:n.*614G=
ENST00000569495.5:n.504G=
ENST00000570063.5:n.1341G=
NM_020317.3:c.704G= NP_064713.3:p.Arg235=
XM_011541797.1:c.704G= XP_011540099.1:p.Arg235=
XM_011541798.1:c.*67G= XP_011540100.1:n.*67G=
XR_241200.1:n.1617G=
XR_241201.1:n.1026G=
XR_946709.1:n.2268G=
XR_946710.1:n.1950G=
XR_946711.1:n.1677G=
XR_946712.1:n.1846G=
XR_946713.1:n.1572G=
NM_001321772.1:c.704G= NP_001308701.1:p.Arg235=
NM_020317.4:c.704G= NP_064713.3:p.Arg235=
NR_135143.1:n.2497G=
NR_135144.1:n.1572G=
NR_135777.1:n.2472G=
NR_135778.1:n.1846G=
NR_135780.1:n.1950G=
NR_135781.1:n.1617G=
NR_135782.1:n.1299G=
NR_135783.1:n.1026G=
NR_135784.1:n.2497G=
NR_135785.1:n.1025G=
NR_135786.1:n.2497G=
NR_135787.1:n.2621G=
NR_135788.1:n.2563G=
NR_135789.1:n.3501G=
XR_946709.2:n.2234G=
NM_020317.5:c.704G= MANE Select NP_064713.3:p.Arg235=
NR_135784.2:n.2432G=
NR_135786.2:n.2432G=
NM_001321772.2:c.704G= NP_001308701.1:p.Arg235=
NR_135143.2:n.2432G=
NR_135144.2:n.1507G=
NR_135777.2:n.2472G=
NR_135778.2:n.1781G=
NR_135780.2:n.1885G=
NR_135781.2:n.1552G=
NR_135782.2:n.1234G=
NR_135783.2:n.961G=
NR_135785.2:n.960G=
NR_135787.2:n.2621G=
NR_135788.2:n.2563G=
NR_135789.2:n.3501G=