Canonical Allele Identifier: CA1009051348

Gene: PRRX1

Linked Data

• dbSNP Id: rs1341299997
• gnomAD v3: 1-170664795-G-T
• gnomAD v4: 1-170664795-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.170664795G>T , CM000663.2:g.170664795G>T	GRCh38
NC_000001.10:g.170633936G>T , CM000663.1:g.170633936G>T	GRCh37
NC_000001.9:g.168900560G>T	NCBI36
NG_031856.2:g.5624G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239461.11:c.241+336G>T MANE Select	ENSP00000239461.6:n.241+336G>T
ENST00000239461.10:c.241+336G>T	ENSP00000239461.6:n.241+336G>T
ENST00000367760.7:c.241+336G>T	ENSP00000356734.3:n.241+336G>T
ENST00000497230.2:c.241+336G>T	ENSP00000450762.1:n.241+336G>T
ENST00000553786.1:n.351+336G>T
NM_006902.4:c.241+336G>T	NP_008833.1:n.241+336G>T
NM_022716.3:c.241+336G>T	NP_073207.1:n.241+336G>T
XM_006711388.2:c.100+336G>T	XP_006711451.1:n.100+336G>T
XM_006711388.3:c.100+336G>T	XP_006711451.1:n.100+336G>T
NM_022716.4:c.241+336G>T MANE Select	NP_073207.1:n.241+336G>T
NM_006902.5:c.241+336G>T	NP_008833.1:n.241+336G>T