Canonical Allele Identifier: CA340729
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8101
dbSNP Id: rs587776682

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177994326_177994338del , CM000667.2:g.177994326_177994338del GRCh38
NC_000005.9:g.177421327_177421339del , CM000667.1:g.177421327_177421339del GRCh37
NC_000005.8:g.177353933_177353945del NCBI36
NG_015889.1:g.6907_6919del

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.112_124del MANE Select ENSP00000311290.2:p.Ser38ProfsTer?
NM_006261.4:c.112_124del NP_006252.3:p.Ser38ProfsTer?
NM_006261.5:c.112_124del MANE Select NP_006252.4:p.Ser38ProfsTer?