Canonical Allele Identifier: CA416726371

Gene: RSRP1

Linked Data

• MyVariant Identifiers: chr1:g.25570094G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25243603G>T , CM000663.2:g.25243603G>T	GRCh38
NC_000001.10:g.25570094G>T , CM000663.1:g.25570094G>T	GRCh37
NC_000001.9:g.25442681G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243189.12:c.703C>A MANE Select	ENSP00000243189.7:p.Arg235=
ENST00000243189.11:c.703C>A	ENSP00000243189.7:p.Arg235=
ENST00000473314.6:c.*658C>A	ENSP00000457582.1:n.*658C>A
ENST00000475766.2:n.254C>A
ENST00000498238.1:n.2431C>A
ENST00000564223.5:n.52C>A
ENST00000565733.5:c.380C>A
ENST00000566395.5:c.320C>A
ENST00000568254.5:c.*613C>A	ENSP00000457195.1:n.*613C>A
ENST00000569495.5:n.503C>A
ENST00000570063.5:n.1340C>A
NM_020317.3:c.703C>A	NP_064713.3:p.Arg235=
XM_011541797.1:c.703C>A	XP_011540099.1:p.Arg235=
XM_011541798.1:c.*66C>A	XP_011540100.1:n.*66C>A
XR_241200.1:n.1616C>A
XR_241201.1:n.1025C>A
XR_946709.1:n.2267C>A
XR_946710.1:n.1949C>A
XR_946711.1:n.1676C>A
XR_946712.1:n.1845C>A
XR_946713.1:n.1571C>A
NM_001321772.1:c.703C>A	NP_001308701.1:p.Arg235=
NM_020317.4:c.703C>A	NP_064713.3:p.Arg235=
NR_135143.1:n.2496C>A
NR_135144.1:n.1571C>A
NR_135777.1:n.2471C>A
NR_135778.1:n.1845C>A
NR_135780.1:n.1949C>A
NR_135781.1:n.1616C>A
NR_135782.1:n.1298C>A
NR_135783.1:n.1025C>A
NR_135784.1:n.2496C>A
NR_135785.1:n.1024C>A
NR_135786.1:n.2496C>A
NR_135787.1:n.2620C>A
NR_135788.1:n.2562C>A
NR_135789.1:n.3500C>A
XR_946709.2:n.2233C>A
NM_020317.5:c.703C>A MANE Select	NP_064713.3:p.Arg235=
NR_135784.2:n.2431C>A
NR_135786.2:n.2431C>A
NM_001321772.2:c.703C>A	NP_001308701.1:p.Arg235=
NR_135143.2:n.2431C>A
NR_135144.2:n.1506C>A
NR_135777.2:n.2471C>A
NR_135778.2:n.1780C>A
NR_135780.2:n.1884C>A
NR_135781.2:n.1551C>A
NR_135782.2:n.1233C>A
NR_135783.2:n.960C>A
NR_135785.2:n.959C>A
NR_135787.2:n.2620C>A
NR_135788.2:n.2562C>A
NR_135789.2:n.3500C>A