Canonical Allele Identifier: CA808117610
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs751165969
MyVariant Identifiers: chr5:g.177419902_177419907del (hg19) chr5:g.177992901_177992906del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992909_177992914del , CM000667.2:g.177992909_177992914del GRCh38
NC_000005.9:g.177419910_177419915del , CM000667.1:g.177419910_177419915del GRCh37
NC_000005.8:g.177352516_177352521del NCBI36
NG_015889.1:g.8337_8342del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.484_489del MANE Select ENSP00000311290.2:p.Pro162_Pro163del
NM_006261.4:c.484_489del NP_006252.3:p.Pro162_Pro163del
NM_006261.5:c.484_489del MANE Select NP_006252.4:p.Pro162_Pro163del
Search 100 bp 5'
Search 100 bp 3'