Canonical Allele Identifier: CA2697395951
Gene: PRRX1 HGNC NCBI

Linked Data

dbSNP Id: rs2101879409

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.170664694C>T , CM000663.2:g.170664694C>T GRCh38
NC_000001.10:g.170633835C>T , CM000663.1:g.170633835C>T GRCh37
NC_000001.9:g.168900459C>T NCBI36
NG_031856.2:g.5523C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239461.11:c.241+235C>T MANE Select ENSP00000239461.6:n.241+235C>T
ENST00000239461.10:c.241+235C>T ENSP00000239461.6:n.241+235C>T
ENST00000367760.7:c.241+235C>T ENSP00000356734.3:n.241+235C>T
ENST00000497230.2:c.241+235C>T ENSP00000450762.1:n.241+235C>T
ENST00000553786.1:n.351+235C>T
NM_006902.4:c.241+235C>T NP_008833.1:n.241+235C>T
NM_022716.3:c.241+235C>T NP_073207.1:n.241+235C>T
XM_006711388.2:c.100+235C>T XP_006711451.1:n.100+235C>T
XM_006711388.3:c.100+235C>T XP_006711451.1:n.100+235C>T
NM_022716.4:c.241+235C>T MANE Select NP_073207.1:n.241+235C>T
NM_006902.5:c.241+235C>T NP_008833.1:n.241+235C>T