Canonical Allele Identifier: CA1139847798

Gene: RSRP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25243590T= , CM000663.2:g.25243590T=	GRCh38
NC_000001.10:g.25570081T= , CM000663.1:g.25570081T=	GRCh37
NC_000001.9:g.25442668T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243189.12:c.716A= MANE Select	ENSP00000243189.7:p.Glu239=
ENST00000243189.11:c.716A=	ENSP00000243189.7:p.Glu239=
ENST00000473314.6:c.*671A=	ENSP00000457582.1:n.*671A=
ENST00000475766.2:n.267A=
ENST00000498238.1:n.2444A=
ENST00000564223.5:n.65A=
ENST00000565733.5:c.393A=
ENST00000566395.5:c.333A=
ENST00000568254.5:c.*626A=	ENSP00000457195.1:n.*626A=
ENST00000569495.5:n.516A=
ENST00000570063.5:n.1353A=
NM_020317.3:c.716A=	NP_064713.3:p.Glu239=
XM_011541797.1:c.716A=	XP_011540099.1:p.Glu239=
XM_011541798.1:c.*79A=	XP_011540100.1:n.*79A=
XR_241200.1:n.1629A=
XR_241201.1:n.1038A=
XR_946709.1:n.2280A=
XR_946710.1:n.1962A=
XR_946711.1:n.1689A=
XR_946712.1:n.1858A=
XR_946713.1:n.1584A=
NM_001321772.1:c.716A=	NP_001308701.1:p.Glu239=
NM_020317.4:c.716A=	NP_064713.3:p.Glu239=
NR_135143.1:n.2509A=
NR_135144.1:n.1584A=
NR_135777.1:n.2484A=
NR_135778.1:n.1858A=
NR_135780.1:n.1962A=
NR_135781.1:n.1629A=
NR_135782.1:n.1311A=
NR_135783.1:n.1038A=
NR_135784.1:n.2509A=
NR_135785.1:n.1037A=
NR_135786.1:n.2509A=
NR_135787.1:n.2633A=
NR_135788.1:n.2575A=
NR_135789.1:n.3513A=
XR_946709.2:n.2246A=
NM_020317.5:c.716A= MANE Select	NP_064713.3:p.Glu239=
NR_135784.2:n.2444A=
NR_135786.2:n.2444A=
NM_001321772.2:c.716A=	NP_001308701.1:p.Glu239=
NR_135143.2:n.2444A=
NR_135144.2:n.1519A=
NR_135777.2:n.2484A=
NR_135778.2:n.1793A=
NR_135780.2:n.1897A=
NR_135781.2:n.1564A=
NR_135782.2:n.1246A=
NR_135783.2:n.973A=
NR_135785.2:n.972A=
NR_135787.2:n.2633A=
NR_135788.2:n.2575A=
NR_135789.2:n.3513A=