Canonical Allele Identifier: CA2769598659
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993199_177993200insACT , CM000667.2:g.177993199_177993200insACT GRCh38
NC_000005.9:g.177420200_177420201insACT , CM000667.1:g.177420200_177420201insACT GRCh37
NC_000005.8:g.177352806_177352807insACT NCBI36
NG_015889.1:g.8043_8044insAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-153_343-152insAGT MANE Select ENSP00000311290.2:n.343-153_343-152insAGT
NM_006261.4:c.343-153_343-152insAGT NP_006252.3:n.343-153_343-152insAGT
NM_006261.5:c.343-153_343-152insAGT MANE Select NP_006252.4:n.343-153_343-152insAGT