Canonical Allele Identifier: CA564901139
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1234884401
gnomAD v2: 5-177419679-TG-T
gnomAD v4: 5-177992678-TG-T
COSMIC: COSN23019094
MyVariant Identifiers: chr5:g.177419680del (hg19) chr5:g.177992679del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992682del , CM000667.2:g.177992682del GRCh38
NC_000005.9:g.177419683del , CM000667.1:g.177419683del GRCh37
NC_000005.8:g.177352289del NCBI36
NG_015889.1:g.8564del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*30del MANE Select ENSP00000311290.2:n.*30del
NM_006261.4:c.*30del NP_006252.3:n.*30del
NM_006261.5:c.*30del MANE Select NP_006252.4:n.*30del
Search 100 bp 5'
Search 100 bp 3'