Canonical Allele Identifier: CA339062768

Gene: RSRP1

Linked Data

• MyVariant Identifiers: chr1:g.25570114T>G (hg19) ; chr1:g.25243623T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25243623T>G , CM000663.2:g.25243623T>G	GRCh38
NC_000001.10:g.25570114T>G , CM000663.1:g.25570114T>G	GRCh37
NC_000001.9:g.25442701T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243189.12:c.683A>C MANE Select	ENSP00000243189.7:p.Lys228Thr
ENST00000243189.11:c.683A>C	ENSP00000243189.7:p.Lys228Thr
ENST00000473314.6:c.*638A>C	ENSP00000457582.1:n.*638A>C
ENST00000475766.2:n.234A>C
ENST00000498238.1:n.2411A>C
ENST00000564223.5:n.32A>C
ENST00000565733.5:c.360A>C
ENST00000566395.5:c.300A>C
ENST00000568254.5:c.*593A>C	ENSP00000457195.1:n.*593A>C
ENST00000569495.5:n.483A>C
ENST00000570063.5:n.1320A>C
NM_020317.3:c.683A>C	NP_064713.3:p.Lys228Thr
XM_011541797.1:c.683A>C	XP_011540099.1:p.Lys228Thr
XM_011541798.1:c.*46A>C	XP_011540100.1:n.*46A>C
XR_241200.1:n.1596A>C
XR_241201.1:n.1005A>C
XR_946709.1:n.2247A>C
XR_946710.1:n.1929A>C
XR_946711.1:n.1656A>C
XR_946712.1:n.1825A>C
XR_946713.1:n.1551A>C
NM_001321772.1:c.683A>C	NP_001308701.1:p.Lys228Thr
NM_020317.4:c.683A>C	NP_064713.3:p.Lys228Thr
NR_135143.1:n.2476A>C
NR_135144.1:n.1551A>C
NR_135777.1:n.2451A>C
NR_135778.1:n.1825A>C
NR_135780.1:n.1929A>C
NR_135781.1:n.1596A>C
NR_135782.1:n.1278A>C
NR_135783.1:n.1005A>C
NR_135784.1:n.2476A>C
NR_135785.1:n.1004A>C
NR_135786.1:n.2476A>C
NR_135787.1:n.2600A>C
NR_135788.1:n.2542A>C
NR_135789.1:n.3480A>C
XR_946709.2:n.2213A>C
NM_020317.5:c.683A>C MANE Select	NP_064713.3:p.Lys228Thr
NR_135784.2:n.2411A>C
NR_135786.2:n.2411A>C
NM_001321772.2:c.683A>C	NP_001308701.1:p.Lys228Thr
NR_135143.2:n.2411A>C
NR_135144.2:n.1486A>C
NR_135777.2:n.2451A>C
NR_135778.2:n.1760A>C
NR_135780.2:n.1864A>C
NR_135781.2:n.1531A>C
NR_135782.2:n.1213A>C
NR_135783.2:n.940A>C
NR_135785.2:n.939A>C
NR_135787.2:n.2600A>C
NR_135788.2:n.2542A>C
NR_135789.2:n.3480A>C