Canonical Allele Identifier: CA339062670

Gene: RSRP1

Linked Data

• gnomAD v4: 1-25243602-C-G
• MyVariant Identifiers: chr1:g.25570093C>G (hg19) ; chr1:g.25243602C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243189.12:c.704G>C MANE Select	ENSP00000243189.7:p.Arg235Pro
ENST00000243189.11:c.704G>C	ENSP00000243189.7:p.Arg235Pro
ENST00000473314.6:c.*659G>C	ENSP00000457582.1:n.*659G>C
ENST00000475766.2:n.255G>C
ENST00000498238.1:n.2432G>C
ENST00000564223.5:n.53G>C
ENST00000565733.5:c.381G>C
ENST00000566395.5:c.321G>C
ENST00000568254.5:c.*614G>C	ENSP00000457195.1:n.*614G>C
ENST00000569495.5:n.504G>C
ENST00000570063.5:n.1341G>C
NM_020317.3:c.704G>C	NP_064713.3:p.Arg235Pro
XM_011541797.1:c.704G>C	XP_011540099.1:p.Arg235Pro
XM_011541798.1:c.*67G>C	XP_011540100.1:n.*67G>C
XR_241200.1:n.1617G>C
XR_241201.1:n.1026G>C
XR_946709.1:n.2268G>C
XR_946710.1:n.1950G>C
XR_946711.1:n.1677G>C
XR_946712.1:n.1846G>C
XR_946713.1:n.1572G>C
NM_001321772.1:c.704G>C	NP_001308701.1:p.Arg235Pro
NM_020317.4:c.704G>C	NP_064713.3:p.Arg235Pro
NR_135143.1:n.2497G>C
NR_135144.1:n.1572G>C
NR_135777.1:n.2472G>C
NR_135778.1:n.1846G>C
NR_135780.1:n.1950G>C
NR_135781.1:n.1617G>C
NR_135782.1:n.1299G>C
NR_135783.1:n.1026G>C
NR_135784.1:n.2497G>C
NR_135785.1:n.1025G>C
NR_135786.1:n.2497G>C
NR_135787.1:n.2621G>C
NR_135788.1:n.2563G>C
NR_135789.1:n.3501G>C
XR_946709.2:n.2234G>C
NM_020317.5:c.704G>C MANE Select	NP_064713.3:p.Arg235Pro
NR_135784.2:n.2432G>C
NR_135786.2:n.2432G>C
NM_001321772.2:c.704G>C	NP_001308701.1:p.Arg235Pro
NR_135143.2:n.2432G>C
NR_135144.2:n.1507G>C
NR_135777.2:n.2472G>C
NR_135778.2:n.1781G>C
NR_135780.2:n.1885G>C
NR_135781.2:n.1552G>C
NR_135782.2:n.1234G>C
NR_135783.2:n.961G>C
NR_135785.2:n.960G>C
NR_135787.2:n.2621G>C
NR_135788.2:n.2563G>C
NR_135789.2:n.3501G>C