Canonical Allele Identifier: CA2651818316
Gene: PROKR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5314262_5314266del , CM000682.2:g.5314262_5314266del GRCh38
NC_000020.10:g.5294908_5294912del , CM000682.1:g.5294908_5294912del GRCh37
NC_000020.9:g.5242908_5242912del NCBI36
NG_008132.1:g.5104_5108del
NG_008132.2:g.5104_5108del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217270.4:c.104_108del ENSP00000217270.3:p.Leu35HisfsTer3
ENST00000678059.1:c.-5_-1del ENSP00000503366.1:n.-5_-1del
ENST00000678254.1:c.104_108del MANE Select ENSP00000504128.1:p.Leu35HisfsTer3
ENST00000217270.3:c.104_108del ENSP00000217270.3:p.Leu35HisfsTer3
NM_144773.2:c.104_108del NP_658986.1:p.Leu35HisfsTer3
XM_005260663.2:c.104_108del XP_005260720.1:p.Leu35HisfsTer3
XM_011529159.1:c.-5_-1del XP_011527461.1:n.-5_-1del
NM_144773.3:c.104_108del NP_658986.1:p.Leu35HisfsTer3
XM_017027646.1:c.104_108del XP_016883135.1:p.Leu35HisfsTer3
NM_144773.4:c.104_108del MANE Select NP_658986.1:p.Leu35HisfsTer3