Canonical Allele Identifier: CA2676774164
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs2113058535
gnomAD v4: 5-177992631-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992634del , CM000667.2:g.177992634del GRCh38
NC_000005.9:g.177419635del , CM000667.1:g.177419635del GRCh37
NC_000005.8:g.177352241del NCBI36
NG_015889.1:g.8611del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*77del MANE Select ENSP00000311290.2:n.*77del
NM_006261.4:c.*77del NP_006252.3:n.*77del
NM_006261.5:c.*77del MANE Select NP_006252.4:n.*77del
Search 100 bp 5'
Search 100 bp 3'