Canonical Allele Identifier: CA1084892859
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1772668400
gnomAD v3: 5-177992812-TC-T
gnomAD v4: 5-177992812-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992814del , CM000667.2:g.177992814del GRCh38
NC_000005.9:g.177419815del , CM000667.1:g.177419815del GRCh37
NC_000005.8:g.177352421del NCBI36
NG_015889.1:g.8430del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.577del MANE Select ENSP00000311290.2:p.Asp193ThrfsTer?
NM_006261.4:c.577del NP_006252.3:p.Asp193ThrfsTer?
NM_006261.5:c.577del MANE Select NP_006252.4:p.Asp193ThrfsTer?
Search 100 bp 5'
Search 100 bp 3'