Canonical Allele Identifier: CA1159576969
Gene: RSRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25243615C= , CM000663.2:g.25243615C= GRCh38
NC_000001.10:g.25570106C= , CM000663.1:g.25570106C= GRCh37
NC_000001.9:g.25442693C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243189.12:c.691G= MANE Select ENSP00000243189.7:p.Glu231=
ENST00000243189.11:c.691G= ENSP00000243189.7:p.Glu231=
ENST00000473314.6:c.*646G= ENSP00000457582.1:n.*646G=
ENST00000475766.2:n.242G=
ENST00000498238.1:n.2419G=
ENST00000564223.5:n.40G=
ENST00000565733.5:c.368G=
ENST00000566395.5:c.308G=
ENST00000568254.5:c.*601G= ENSP00000457195.1:n.*601G=
ENST00000569495.5:n.491G=
ENST00000570063.5:n.1328G=
NM_020317.3:c.691G= NP_064713.3:p.Glu231=
XM_011541797.1:c.691G= XP_011540099.1:p.Glu231=
XM_011541798.1:c.*54G= XP_011540100.1:n.*54G=
XR_241200.1:n.1604G=
XR_241201.1:n.1013G=
XR_946709.1:n.2255G=
XR_946710.1:n.1937G=
XR_946711.1:n.1664G=
XR_946712.1:n.1833G=
XR_946713.1:n.1559G=
NM_001321772.1:c.691G= NP_001308701.1:p.Glu231=
NM_020317.4:c.691G= NP_064713.3:p.Glu231=
NR_135143.1:n.2484G=
NR_135144.1:n.1559G=
NR_135777.1:n.2459G=
NR_135778.1:n.1833G=
NR_135780.1:n.1937G=
NR_135781.1:n.1604G=
NR_135782.1:n.1286G=
NR_135783.1:n.1013G=
NR_135784.1:n.2484G=
NR_135785.1:n.1012G=
NR_135786.1:n.2484G=
NR_135787.1:n.2608G=
NR_135788.1:n.2550G=
NR_135789.1:n.3488G=
XR_946709.2:n.2221G=
NM_020317.5:c.691G= MANE Select NP_064713.3:p.Glu231=
NR_135784.2:n.2419G=
NR_135786.2:n.2419G=
NM_001321772.2:c.691G= NP_001308701.1:p.Glu231=
NR_135143.2:n.2419G=
NR_135144.2:n.1494G=
NR_135777.2:n.2459G=
NR_135778.2:n.1768G=
NR_135780.2:n.1872G=
NR_135781.2:n.1539G=
NR_135782.2:n.1221G=
NR_135783.2:n.948G=
NR_135785.2:n.947G=
NR_135787.2:n.2608G=
NR_135788.2:n.2550G=
NR_135789.2:n.3488G=