Canonical Allele Identifier: CA2347441738
Gene: PROKR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5314249C= , CM000682.2:g.5314249C= GRCh38
NC_000020.10:g.5294895C= , CM000682.1:g.5294895C= GRCh37
NC_000020.9:g.5242895C= NCBI36
NG_008132.1:g.5121G=
NG_008132.2:g.5121G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217270.4:c.121G= ENSP00000217270.3:p.Glu41=
ENST00000678059.1:c.13G= ENSP00000503366.1:p.Glu5=
ENST00000678254.1:c.121G= MANE Select ENSP00000504128.1:p.Glu41=
ENST00000217270.3:c.121G= ENSP00000217270.3:p.Glu41=
NM_144773.2:c.121G= NP_658986.1:p.Glu41=
XM_005260663.2:c.121G= XP_005260720.1:p.Glu41=
XM_011529159.1:c.13G= XP_011527461.1:p.Glu5=
NM_144773.3:c.121G= NP_658986.1:p.Glu41=
XM_017027646.1:c.121G= XP_016883135.1:p.Glu41=
NM_144773.4:c.121G= MANE Select NP_658986.1:p.Glu41=