Canonical Allele Identifier: CA2676774763
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992765-G-GCT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992765_177992766insCT , CM000667.2:g.177992765_177992766insCT GRCh38
NC_000005.9:g.177419766_177419767insCT , CM000667.1:g.177419766_177419767insCT GRCh37
NC_000005.8:g.177352372_177352373insCT NCBI36
NG_015889.1:g.8477_8478insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.624_625insAG MANE Select ENSP00000311290.2:p.Pro209SerfsTer28
NM_006261.4:c.624_625insAG NP_006252.3:p.Pro209SerfsTer28
NM_006261.5:c.624_625insAG MANE Select NP_006252.4:p.Pro209SerfsTer28
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Search 100 bp 3'