Canonical Allele Identifier: CA339062703

Gene: RSRP1

Linked Data

• MyVariant Identifiers: chr1:g.25570101A>T (hg19) ; chr1:g.25243610A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25243610A>T , CM000663.2:g.25243610A>T	GRCh38
NC_000001.10:g.25570101A>T , CM000663.1:g.25570101A>T	GRCh37
NC_000001.9:g.25442688A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243189.12:c.696T>A MANE Select	ENSP00000243189.7:p.Asp232Glu
ENST00000243189.11:c.696T>A	ENSP00000243189.7:p.Asp232Glu
ENST00000473314.6:c.*651T>A	ENSP00000457582.1:n.*651T>A
ENST00000475766.2:n.247T>A
ENST00000498238.1:n.2424T>A
ENST00000564223.5:n.45T>A
ENST00000565733.5:c.373T>A
ENST00000566395.5:c.313T>A
ENST00000568254.5:c.*606T>A	ENSP00000457195.1:n.*606T>A
ENST00000569495.5:n.496T>A
ENST00000570063.5:n.1333T>A
NM_020317.3:c.696T>A	NP_064713.3:p.Asp232Glu
XM_011541797.1:c.696T>A	XP_011540099.1:p.Asp232Glu
XM_011541798.1:c.*59T>A	XP_011540100.1:n.*59T>A
XR_241200.1:n.1609T>A
XR_241201.1:n.1018T>A
XR_946709.1:n.2260T>A
XR_946710.1:n.1942T>A
XR_946711.1:n.1669T>A
XR_946712.1:n.1838T>A
XR_946713.1:n.1564T>A
NM_001321772.1:c.696T>A	NP_001308701.1:p.Asp232Glu
NM_020317.4:c.696T>A	NP_064713.3:p.Asp232Glu
NR_135143.1:n.2489T>A
NR_135144.1:n.1564T>A
NR_135777.1:n.2464T>A
NR_135778.1:n.1838T>A
NR_135780.1:n.1942T>A
NR_135781.1:n.1609T>A
NR_135782.1:n.1291T>A
NR_135783.1:n.1018T>A
NR_135784.1:n.2489T>A
NR_135785.1:n.1017T>A
NR_135786.1:n.2489T>A
NR_135787.1:n.2613T>A
NR_135788.1:n.2555T>A
NR_135789.1:n.3493T>A
XR_946709.2:n.2226T>A
NM_020317.5:c.696T>A MANE Select	NP_064713.3:p.Asp232Glu
NR_135784.2:n.2424T>A
NR_135786.2:n.2424T>A
NM_001321772.2:c.696T>A	NP_001308701.1:p.Asp232Glu
NR_135143.2:n.2424T>A
NR_135144.2:n.1499T>A
NR_135777.2:n.2464T>A
NR_135778.2:n.1773T>A
NR_135780.2:n.1877T>A
NR_135781.2:n.1544T>A
NR_135782.2:n.1226T>A
NR_135783.2:n.953T>A
NR_135785.2:n.952T>A
NR_135787.2:n.2613T>A
NR_135788.2:n.2555T>A
NR_135789.2:n.3493T>A