Canonical Allele Identifier: CA2676773869
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992505-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992507del , CM000667.2:g.177992507del GRCh38
NC_000005.9:g.177419508del , CM000667.1:g.177419508del GRCh37
NC_000005.8:g.177352114del NCBI36
NG_015889.1:g.8737del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*203del MANE Select ENSP00000311290.2:n.*203del
NM_006261.4:c.*203del NP_006252.3:n.*203del
NM_006261.5:c.*203del MANE Select NP_006252.4:n.*203del
Search 100 bp 5'
Search 100 bp 3'