Canonical Allele Identifier: CA2347441727
Gene: PROKR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5314227_5314228delinsGT , CM000682.2:g.5314227_5314228delinsGT GRCh38
NC_000020.10:g.5294873_5294874delinsGT , CM000682.1:g.5294873_5294874delinsGT GRCh37
NC_000020.9:g.5242873_5242874delinsGT NCBI36
NG_008132.1:g.5142_5143delinsAC
NG_008132.2:g.5142_5143delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000217270.4:c.142_143delinsAC ENSP00000217270.3:p.Thr48=
ENST00000678059.1:c.34_35delinsAC ENSP00000503366.1:p.Thr12=
ENST00000678254.1:c.142_143delinsAC MANE Select ENSP00000504128.1:p.Thr48=
ENST00000217270.3:c.142_143delinsAC ENSP00000217270.3:p.Thr48=
NM_144773.2:c.142_143delinsAC NP_658986.1:p.Thr48=
XM_005260663.2:c.142_143delinsAC XP_005260720.1:p.Thr48=
XM_011529159.1:c.34_35delinsAC XP_011527461.1:p.Thr12=
NM_144773.3:c.142_143delinsAC NP_658986.1:p.Thr48=
XM_017027646.1:c.142_143delinsAC XP_016883135.1:p.Thr48=
NM_144773.4:c.142_143delinsAC MANE Select NP_658986.1:p.Thr48=