Canonical Allele Identifier: CA808117069
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1170598288
gnomAD v3: 5-177992515-CA-C
gnomAD v4: 5-177992515-CA-C
MyVariant Identifiers: chr5:g.177419517del (hg19) chr5:g.177992516del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992516del , CM000667.2:g.177992516del GRCh38
NC_000005.9:g.177419517del , CM000667.1:g.177419517del GRCh37
NC_000005.8:g.177352123del NCBI36
NG_015889.1:g.8727del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*193del MANE Select ENSP00000311290.2:n.*193del
NM_006261.4:c.*193del NP_006252.3:n.*193del
NM_006261.5:c.*193del MANE Select NP_006252.4:n.*193del
Search 100 bp 5'
Search 100 bp 3'