Canonical Allele Identifier: CA2580074075
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2127143
ClinVar RCV Id: RCV003052016

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992927del , CM000667.2:g.177992927del GRCh38
NC_000005.9:g.177419928del , CM000667.1:g.177419928del GRCh37
NC_000005.8:g.177352534del NCBI36
NG_015889.1:g.8316del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.463del MANE Select ENSP00000311290.2:p.Tyr155IlefsTer10
NM_006261.4:c.463del NP_006252.3:p.Tyr155IlefsTer10
NM_006261.5:c.463del MANE Select NP_006252.4:p.Tyr155IlefsTer10