Canonical Allele Identifier: CA1206602999

Gene: PRRX1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.170664754_170664755delinsCT , CM000663.2:g.170664754_170664755delinsCT	GRCh38
NC_000001.10:g.170633895_170633896delinsCT , CM000663.1:g.170633895_170633896delinsCT	GRCh37
NC_000001.9:g.168900519_168900520delinsCT	NCBI36
NG_031856.2:g.5583_5584delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239461.11:c.241+295_241+296delinsCT MANE Select	ENSP00000239461.6:n.241+295_241+296delinsCT
ENST00000239461.10:c.241+295_241+296delinsCT	ENSP00000239461.6:n.241+295_241+296delinsCT
ENST00000367760.7:c.241+295_241+296delinsCT	ENSP00000356734.3:n.241+295_241+296delinsCT
ENST00000497230.2:c.241+295_241+296delinsCT	ENSP00000450762.1:n.241+295_241+296delinsCT
ENST00000553786.1:n.351+295_351+296delinsCT
NM_006902.4:c.241+295_241+296delinsCT	NP_008833.1:n.241+295_241+296delinsCT
NM_022716.3:c.241+295_241+296delinsCT	NP_073207.1:n.241+295_241+296delinsCT
XM_006711388.2:c.100+295_100+296delinsCT	XP_006711451.1:n.100+295_100+296delinsCT
XM_006711388.3:c.100+295_100+296delinsCT	XP_006711451.1:n.100+295_100+296delinsCT
NM_022716.4:c.241+295_241+296delinsCT MANE Select	NP_073207.1:n.241+295_241+296delinsCT
NM_006902.5:c.241+295_241+296delinsCT	NP_008833.1:n.241+295_241+296delinsCT