Canonical Allele Identifier: CA1206603019

Gene: PRRX1

Linked Data

• dbSNP Id: rs1652859805

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.170664786G>C , CM000663.2:g.170664786G>C	GRCh38
NC_000001.10:g.170633927G>C , CM000663.1:g.170633927G>C	GRCh37
NC_000001.9:g.168900551G>C	NCBI36
NG_031856.2:g.5615G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239461.11:c.241+327G>C MANE Select	ENSP00000239461.6:n.241+327G>C
ENST00000239461.10:c.241+327G>C	ENSP00000239461.6:n.241+327G>C
ENST00000367760.7:c.241+327G>C	ENSP00000356734.3:n.241+327G>C
ENST00000497230.2:c.241+327G>C	ENSP00000450762.1:n.241+327G>C
ENST00000553786.1:n.351+327G>C
NM_006902.4:c.241+327G>C	NP_008833.1:n.241+327G>C
NM_022716.3:c.241+327G>C	NP_073207.1:n.241+327G>C
XM_006711388.2:c.100+327G>C	XP_006711451.1:n.100+327G>C
XM_006711388.3:c.100+327G>C	XP_006711451.1:n.100+327G>C
NM_022716.4:c.241+327G>C MANE Select	NP_073207.1:n.241+327G>C
NM_006902.5:c.241+327G>C	NP_008833.1:n.241+327G>C