Canonical Allele Identifier: CA7154898

Gene: PRORP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35266752C>A , CM000676.2:g.35266752C>A	GRCh38
NC_000014.8:g.35735958C>A , CM000676.1:g.35735958C>A	GRCh37
NC_000014.7:g.34805709C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014672.4:c.1301C>A MANE Select	NP_055487.2:p.Ala434Asp
ENST00000534898.9:c.1301C>A MANE Select	ENSP00000440915.2:p.Ala434Asp
NM_001256678.1:c.1253C>A	NP_001243607.1:p.Ala418Asp
NM_001256678.2:c.1253C>A	NP_001243607.1:p.Ala418Asp
NM_001256679.1:c.1016C>A	NP_001243608.1:p.Ala339Asp
NM_001256679.2:c.1016C>A	NP_001243608.1:p.Ala339Asp
NM_001256680.1:c.185C>A	NP_001243609.1:p.Ala62Asp
NM_001256680.2:c.185C>A	NP_001243609.1:p.Ala62Asp
NM_001256681.1:c.185C>A	NP_001243610.1:p.Ala62Asp
NM_001256681.2:c.185C>A	NP_001243610.1:p.Ala62Asp
NM_014672.3:c.1301C>A	NP_055487.2:p.Ala434Asp
ENST00000250377.11:c.1253C>A	ENSP00000250377.8:p.Ala418Asp
ENST00000321130.14:c.185C>A	ENSP00000324697.9:p.Ala62Asp
ENST00000534898.8:c.1301C>A	ENSP00000440915.2:p.Ala434Asp
ENST00000557404.3:c.185C>A	ENSP00000450898.3:p.Ala62Asp
ENST00000557565.1:c.1301C>A	ENSP00000454657.1:p.Ala434Asp
ENST00000603544.5:c.1253C>A	ENSP00000473856.1:p.Ala418Asp
ENST00000604948.5:c.1016C>A	ENSP00000474620.1:p.Ala339Asp
ENST00000605870.5:c.185C>A	ENSP00000474299.1:p.Ala62Asp
XM_005268237.2:c.1301C>A	XP_005268294.1:p.Ala434Asp
XM_005268237.3:c.1301C>A	XP_005268294.1:p.Ala434Asp
XM_011537409.1:c.1301C>A	XP_011535711.1:p.Ala434Asp
XM_011537410.1:c.1301C>A	XP_011535712.1:p.Ala434Asp
XM_011537410.2:c.1301C>A	XP_011535712.1:p.Ala434Asp
XM_011537411.1:c.1301C>A	XP_011535713.1:p.Ala434Asp
XM_017021836.1:c.1253C>A	XP_016877325.1:p.Ala418Asp