Canonical Allele Identifier: CA416726364

Gene: RSRP1

Linked Data

• MyVariant Identifiers: chr1:g.25570092T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25243601T>G , CM000663.2:g.25243601T>G	GRCh38
NC_000001.10:g.25570092T>G , CM000663.1:g.25570092T>G	GRCh37
NC_000001.9:g.25442679T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000243189.12:c.705A>C MANE Select	ENSP00000243189.7:p.Arg235=
ENST00000243189.11:c.705A>C	ENSP00000243189.7:p.Arg235=
ENST00000473314.6:c.*660A>C	ENSP00000457582.1:n.*660A>C
ENST00000475766.2:n.256A>C
ENST00000498238.1:n.2433A>C
ENST00000564223.5:n.54A>C
ENST00000565733.5:c.382A>C
ENST00000566395.5:c.322A>C
ENST00000568254.5:c.*615A>C	ENSP00000457195.1:n.*615A>C
ENST00000569495.5:n.505A>C
ENST00000570063.5:n.1342A>C
NM_020317.3:c.705A>C	NP_064713.3:p.Arg235=
XM_011541797.1:c.705A>C	XP_011540099.1:p.Arg235=
XM_011541798.1:c.*68A>C	XP_011540100.1:n.*68A>C
XR_241200.1:n.1618A>C
XR_241201.1:n.1027A>C
XR_946709.1:n.2269A>C
XR_946710.1:n.1951A>C
XR_946711.1:n.1678A>C
XR_946712.1:n.1847A>C
XR_946713.1:n.1573A>C
NM_001321772.1:c.705A>C	NP_001308701.1:p.Arg235=
NM_020317.4:c.705A>C	NP_064713.3:p.Arg235=
NR_135143.1:n.2498A>C
NR_135144.1:n.1573A>C
NR_135777.1:n.2473A>C
NR_135778.1:n.1847A>C
NR_135780.1:n.1951A>C
NR_135781.1:n.1618A>C
NR_135782.1:n.1300A>C
NR_135783.1:n.1027A>C
NR_135784.1:n.2498A>C
NR_135785.1:n.1026A>C
NR_135786.1:n.2498A>C
NR_135787.1:n.2622A>C
NR_135788.1:n.2564A>C
NR_135789.1:n.3502A>C
XR_946709.2:n.2235A>C
NM_020317.5:c.705A>C MANE Select	NP_064713.3:p.Arg235=
NR_135784.2:n.2433A>C
NR_135786.2:n.2433A>C
NM_001321772.2:c.705A>C	NP_001308701.1:p.Arg235=
NR_135143.2:n.2433A>C
NR_135144.2:n.1508A>C
NR_135777.2:n.2473A>C
NR_135778.2:n.1782A>C
NR_135780.2:n.1886A>C
NR_135781.2:n.1553A>C
NR_135782.2:n.1235A>C
NR_135783.2:n.962A>C
NR_135785.2:n.961A>C
NR_135787.2:n.2622A>C
NR_135788.2:n.2564A>C
NR_135789.2:n.3502A>C