Canonical Allele Identifier: CA2676773877
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992512-G-GACCTGCTTCC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992512_177992513insACCTGCTTCC , CM000667.2:g.177992512_177992513insACCTGCTTCC GRCh38
NC_000005.9:g.177419513_177419514insACCTGCTTCC , CM000667.1:g.177419513_177419514insACCTGCTTCC GRCh37
NC_000005.8:g.177352119_177352120insACCTGCTTCC NCBI36
NG_015889.1:g.8730_8731insGGAAGCAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*196_*197insGGAAGCAGGT MANE Select ENSP00000311290.2:n.*196_*197insGGAAGCAGGT
NM_006261.4:c.*196_*197insGGAAGCAGGT NP_006252.3:n.*196_*197insGGAAGCAGGT
NM_006261.5:c.*196_*197insGGAAGCAGGT MANE Select NP_006252.4:n.*196_*197insGGAAGCAGGT
Search 100 bp 5'
Search 100 bp 3'