Canonical Allele Identifier: CA339062642

Gene: RSRP1

Linked Data

• MyVariant Identifiers: chr1:g.25570087G>T (hg19) ; chr1:g.25243596G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25243596G>T , CM000663.2:g.25243596G>T	GRCh38
NC_000001.10:g.25570087G>T , CM000663.1:g.25570087G>T	GRCh37
NC_000001.9:g.25442674G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000243189.12:c.710C>A MANE Select	ENSP00000243189.7:p.Pro237His
ENST00000243189.11:c.710C>A	ENSP00000243189.7:p.Pro237His
ENST00000473314.6:c.*665C>A	ENSP00000457582.1:n.*665C>A
ENST00000475766.2:n.261C>A
ENST00000498238.1:n.2438C>A
ENST00000564223.5:n.59C>A
ENST00000565733.5:c.387C>A
ENST00000566395.5:c.327C>A
ENST00000568254.5:c.*620C>A	ENSP00000457195.1:n.*620C>A
ENST00000569495.5:n.510C>A
ENST00000570063.5:n.1347C>A
NM_020317.3:c.710C>A	NP_064713.3:p.Pro237His
XM_011541797.1:c.710C>A	XP_011540099.1:p.Pro237His
XM_011541798.1:c.*73C>A	XP_011540100.1:n.*73C>A
XR_241200.1:n.1623C>A
XR_241201.1:n.1032C>A
XR_946709.1:n.2274C>A
XR_946710.1:n.1956C>A
XR_946711.1:n.1683C>A
XR_946712.1:n.1852C>A
XR_946713.1:n.1578C>A
NM_001321772.1:c.710C>A	NP_001308701.1:p.Pro237His
NM_020317.4:c.710C>A	NP_064713.3:p.Pro237His
NR_135143.1:n.2503C>A
NR_135144.1:n.1578C>A
NR_135777.1:n.2478C>A
NR_135778.1:n.1852C>A
NR_135780.1:n.1956C>A
NR_135781.1:n.1623C>A
NR_135782.1:n.1305C>A
NR_135783.1:n.1032C>A
NR_135784.1:n.2503C>A
NR_135785.1:n.1031C>A
NR_135786.1:n.2503C>A
NR_135787.1:n.2627C>A
NR_135788.1:n.2569C>A
NR_135789.1:n.3507C>A
XR_946709.2:n.2240C>A
NM_020317.5:c.710C>A MANE Select	NP_064713.3:p.Pro237His
NR_135784.2:n.2438C>A
NR_135786.2:n.2438C>A
NM_001321772.2:c.710C>A	NP_001308701.1:p.Pro237His
NR_135143.2:n.2438C>A
NR_135144.2:n.1513C>A
NR_135777.2:n.2478C>A
NR_135778.2:n.1787C>A
NR_135780.2:n.1891C>A
NR_135781.2:n.1558C>A
NR_135782.2:n.1240C>A
NR_135783.2:n.967C>A
NR_135785.2:n.966C>A
NR_135787.2:n.2627C>A
NR_135788.2:n.2569C>A
NR_135789.2:n.3507C>A