Canonical Allele Identifier: CA2676773925
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992531-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992532del , CM000667.2:g.177992532del GRCh38
NC_000005.9:g.177419533del , CM000667.1:g.177419533del GRCh37
NC_000005.8:g.177352139del NCBI36
NG_015889.1:g.8711del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*177del MANE Select ENSP00000311290.2:n.*177del
NM_006261.4:c.*177del NP_006252.3:n.*177del
NM_006261.5:c.*177del MANE Select NP_006252.4:n.*177del
Search 100 bp 5'
Search 100 bp 3'