Canonical Allele Identifier: CA2676774002
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992568_177992569insA , CM000667.2:g.177992568_177992569insA GRCh38
NC_000005.9:g.177419569_177419570insA , CM000667.1:g.177419569_177419570insA GRCh37
NC_000005.8:g.177352175_177352176insA NCBI36
NG_015889.1:g.8674_8675insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*140_*141insT MANE Select ENSP00000311290.2:n.*140_*141insT
NM_006261.4:c.*140_*141insT NP_006252.3:n.*140_*141insT
NM_006261.5:c.*140_*141insT MANE Select NP_006252.4:n.*140_*141insT