Canonical Allele Identifier: CA408168287
Gene: PROKR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5314220G>T , CM000682.2:g.5314220G>T GRCh38
NC_000020.10:g.5294866G>T , CM000682.1:g.5294866G>T GRCh37
NC_000020.9:g.5242866G>T NCBI36
NG_008132.1:g.5150C>A
NG_008132.2:g.5150C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217270.4:c.150C>A ENSP00000217270.3:p.Phe50Leu
ENST00000678059.1:c.42C>A ENSP00000503366.1:p.Phe14Leu
ENST00000678254.1:c.150C>A MANE Select ENSP00000504128.1:p.Phe50Leu
ENST00000217270.3:c.150C>A ENSP00000217270.3:p.Phe50Leu
NM_144773.2:c.150C>A NP_658986.1:p.Phe50Leu
XM_005260663.2:c.150C>A XP_005260720.1:p.Phe50Leu
XM_011529159.1:c.42C>A XP_011527461.1:p.Phe14Leu
NM_144773.3:c.150C>A NP_658986.1:p.Phe50Leu
XM_017027646.1:c.150C>A XP_016883135.1:p.Phe50Leu
NM_144773.4:c.150C>A MANE Select NP_658986.1:p.Phe50Leu