Canonical Allele Identifier: CA1139820524
Gene: PRRX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.170664755T= , CM000663.2:g.170664755T= GRCh38
NC_000001.10:g.170633896T= , CM000663.1:g.170633896T= GRCh37
NC_000001.9:g.168900520T= NCBI36
NG_031856.2:g.5584T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239461.11:c.241+296T= MANE Select ENSP00000239461.6:n.241+296T=
ENST00000239461.10:c.241+296T= ENSP00000239461.6:n.241+296T=
ENST00000367760.7:c.241+296T= ENSP00000356734.3:n.241+296T=
ENST00000497230.2:c.241+296T= ENSP00000450762.1:n.241+296T=
ENST00000553786.1:n.351+296T=
NM_006902.4:c.241+296T= NP_008833.1:n.241+296T=
NM_022716.3:c.241+296T= NP_073207.1:n.241+296T=
XM_006711388.2:c.100+296T= XP_006711451.1:n.100+296T=
XM_006711388.3:c.100+296T= XP_006711451.1:n.100+296T=
NM_022716.4:c.241+296T= MANE Select NP_073207.1:n.241+296T=
NM_006902.5:c.241+296T= NP_008833.1:n.241+296T=