Canonical Allele Identifier: CA416726339

Gene: RSRP1

Linked Data

• MyVariant Identifiers: chr1:g.25570086G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25243595G>T , CM000663.2:g.25243595G>T	GRCh38
NC_000001.10:g.25570086G>T , CM000663.1:g.25570086G>T	GRCh37
NC_000001.9:g.25442673G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000243189.12:c.711C>A MANE Select	ENSP00000243189.7:p.Pro237=
ENST00000243189.11:c.711C>A	ENSP00000243189.7:p.Pro237=
ENST00000473314.6:c.*666C>A	ENSP00000457582.1:n.*666C>A
ENST00000475766.2:n.262C>A
ENST00000498238.1:n.2439C>A
ENST00000564223.5:n.60C>A
ENST00000565733.5:c.388C>A
ENST00000566395.5:c.328C>A
ENST00000568254.5:c.*621C>A	ENSP00000457195.1:n.*621C>A
ENST00000569495.5:n.511C>A
ENST00000570063.5:n.1348C>A
NM_020317.3:c.711C>A	NP_064713.3:p.Pro237=
XM_011541797.1:c.711C>A	XP_011540099.1:p.Pro237=
XM_011541798.1:c.*74C>A	XP_011540100.1:n.*74C>A
XR_241200.1:n.1624C>A
XR_241201.1:n.1033C>A
XR_946709.1:n.2275C>A
XR_946710.1:n.1957C>A
XR_946711.1:n.1684C>A
XR_946712.1:n.1853C>A
XR_946713.1:n.1579C>A
NM_001321772.1:c.711C>A	NP_001308701.1:p.Pro237=
NM_020317.4:c.711C>A	NP_064713.3:p.Pro237=
NR_135143.1:n.2504C>A
NR_135144.1:n.1579C>A
NR_135777.1:n.2479C>A
NR_135778.1:n.1853C>A
NR_135780.1:n.1957C>A
NR_135781.1:n.1624C>A
NR_135782.1:n.1306C>A
NR_135783.1:n.1033C>A
NR_135784.1:n.2504C>A
NR_135785.1:n.1032C>A
NR_135786.1:n.2504C>A
NR_135787.1:n.2628C>A
NR_135788.1:n.2570C>A
NR_135789.1:n.3508C>A
XR_946709.2:n.2241C>A
NM_020317.5:c.711C>A MANE Select	NP_064713.3:p.Pro237=
NR_135784.2:n.2439C>A
NR_135786.2:n.2439C>A
NM_001321772.2:c.711C>A	NP_001308701.1:p.Pro237=
NR_135143.2:n.2439C>A
NR_135144.2:n.1514C>A
NR_135777.2:n.2479C>A
NR_135778.2:n.1788C>A
NR_135780.2:n.1892C>A
NR_135781.2:n.1559C>A
NR_135782.2:n.1241C>A
NR_135783.2:n.968C>A
NR_135785.2:n.967C>A
NR_135787.2:n.2628C>A
NR_135788.2:n.2570C>A
NR_135789.2:n.3508C>A