Canonical Allele Identifier: CA408168400
Gene: PROKR2 HGNC NCBI

Linked Data

dbSNP Id: rs1232678900
gnomAD v2: 20-5294916-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5314270C>T , CM000682.2:g.5314270C>T GRCh38
NC_000020.10:g.5294916C>T , CM000682.1:g.5294916C>T GRCh37
NC_000020.9:g.5242916C>T NCBI36
NG_008132.1:g.5100G>A
NG_008132.2:g.5100G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217270.4:c.100G>A ENSP00000217270.3:p.Asp34Asn
ENST00000678059.1:c.-9G>A ENSP00000503366.1:n.-9G>A
ENST00000678254.1:c.100G>A MANE Select ENSP00000504128.1:p.Asp34Asn
ENST00000217270.3:c.100G>A ENSP00000217270.3:p.Asp34Asn
NM_144773.2:c.100G>A NP_658986.1:p.Asp34Asn
XM_005260663.2:c.100G>A XP_005260720.1:p.Asp34Asn
XM_011529159.1:c.-9G>A XP_011527461.1:n.-9G>A
NM_144773.3:c.100G>A NP_658986.1:p.Asp34Asn
XM_017027646.1:c.100G>A XP_016883135.1:p.Asp34Asn
NM_144773.4:c.100G>A MANE Select NP_658986.1:p.Asp34Asn