Canonical Allele Identifier: CA2676773988
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992564_177992565insGAA , CM000667.2:g.177992564_177992565insGAA GRCh38
NC_000005.9:g.177419565_177419566insGAA , CM000667.1:g.177419565_177419566insGAA GRCh37
NC_000005.8:g.177352171_177352172insGAA NCBI36
NG_015889.1:g.8679_8680insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*145_*146insTCT MANE Select ENSP00000311290.2:n.*145_*146insTCT
NM_006261.4:c.*145_*146insTCT NP_006252.3:n.*145_*146insTCT
NM_006261.5:c.*145_*146insTCT MANE Select NP_006252.4:n.*145_*146insTCT