Canonical Allele Identifier: CA2676773880
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992513_177992514insA , CM000667.2:g.177992513_177992514insA GRCh38
NC_000005.9:g.177419514_177419515insA , CM000667.1:g.177419514_177419515insA GRCh37
NC_000005.8:g.177352120_177352121insA NCBI36
NG_015889.1:g.8729_8730insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*195_*196insT MANE Select ENSP00000311290.2:n.*195_*196insT
NM_006261.4:c.*195_*196insT NP_006252.3:n.*195_*196insT
NM_006261.5:c.*195_*196insT MANE Select NP_006252.4:n.*195_*196insT