Canonical Allele Identifier: CA1206602972
Gene: PRRX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.170664698G= , CM000663.2:g.170664698G= GRCh38
NC_000001.10:g.170633839G= , CM000663.1:g.170633839G= GRCh37
NC_000001.9:g.168900463G= NCBI36
NG_031856.2:g.5527G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239461.11:c.241+239G= MANE Select ENSP00000239461.6:n.241+239G=
ENST00000239461.10:c.241+239G= ENSP00000239461.6:n.241+239G=
ENST00000367760.7:c.241+239G= ENSP00000356734.3:n.241+239G=
ENST00000497230.2:c.241+239G= ENSP00000450762.1:n.241+239G=
ENST00000553786.1:n.351+239G=
NM_006902.4:c.241+239G= NP_008833.1:n.241+239G=
NM_022716.3:c.241+239G= NP_073207.1:n.241+239G=
XM_006711388.2:c.100+239G= XP_006711451.1:n.100+239G=
XM_006711388.3:c.100+239G= XP_006711451.1:n.100+239G=
NM_022716.4:c.241+239G= MANE Select NP_073207.1:n.241+239G=
NM_006902.5:c.241+239G= NP_008833.1:n.241+239G=
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