Canonical Allele Identifier: CA1603814029
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992900_177992906delinsCTGGTGG , CM000667.2:g.177992900_177992906delinsCTGGTGG GRCh38
NC_000005.9:g.177419901_177419907delinsCTGGTGG , CM000667.1:g.177419901_177419907delinsCTGGTGG GRCh37
NC_000005.8:g.177352507_177352513delinsCTGGTGG NCBI36
NG_015889.1:g.8337_8343delinsCCACCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.484_490delinsCCACCAG MANE Select ENSP00000311290.2:p.Pro162=
NM_006261.4:c.484_490delinsCCACCAG NP_006252.3:p.Pro162=
NM_006261.5:c.484_490delinsCCACCAG MANE Select NP_006252.4:p.Pro162=