Canonical Allele Identifier: CA2347441748
Gene: PROKR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5314265_5314270delinsGAGGTC , CM000682.2:g.5314265_5314270delinsGAGGTC GRCh38
NC_000020.10:g.5294911_5294916delinsGAGGTC , CM000682.1:g.5294911_5294916delinsGAGGTC GRCh37
NC_000020.9:g.5242911_5242916delinsGAGGTC NCBI36
NG_008132.1:g.5100_5105delinsGACCTC
NG_008132.2:g.5100_5105delinsGACCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000217270.4:c.100_105delinsGACCTC ENSP00000217270.3:p.Asp34=
ENST00000678059.1:c.-9_-4delinsGACCTC ENSP00000503366.1:n.-9_-4delinsGACCTC
ENST00000678254.1:c.100_105delinsGACCTC MANE Select ENSP00000504128.1:p.Asp34=
ENST00000217270.3:c.100_105delinsGACCTC ENSP00000217270.3:p.Asp34=
NM_144773.2:c.100_105delinsGACCTC NP_658986.1:p.Asp34=
XM_005260663.2:c.100_105delinsGACCTC XP_005260720.1:p.Asp34=
XM_011529159.1:c.-9_-4delinsGACCTC XP_011527461.1:n.-9_-4delinsGACCTC
NM_144773.3:c.100_105delinsGACCTC NP_658986.1:p.Asp34=
XM_017027646.1:c.100_105delinsGACCTC XP_016883135.1:p.Asp34=
NM_144773.4:c.100_105delinsGACCTC MANE Select NP_658986.1:p.Asp34=