Canonical Allele Identifier: CA2676775218
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993080_177993081insCT , CM000667.2:g.177993080_177993081insCT GRCh38
NC_000005.9:g.177420081_177420082insCT , CM000667.1:g.177420081_177420082insCT GRCh37
NC_000005.8:g.177352687_177352688insCT NCBI36
NG_015889.1:g.8162_8163insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-34_343-33insAG MANE Select ENSP00000311290.2:n.343-34_343-33insAG
NM_006261.4:c.343-34_343-33insAG NP_006252.3:n.343-34_343-33insAG
NM_006261.5:c.343-34_343-33insAG MANE Select NP_006252.4:n.343-34_343-33insAG