Canonical Allele Identifier: CA447992865
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2814627
ClinVar RCV Id: RCV003683017
MyVariant Identifiers: chr5:g.177422836G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995835G>T , CM000667.2:g.177995835G>T GRCh38
NC_000005.9:g.177422836G>T , CM000667.1:g.177422836G>T GRCh37
NC_000005.8:g.177355442G>T NCBI36
NG_015889.1:g.5408C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.99C>A MANE Select ENSP00000311290.2:p.Thr33=
NM_006261.4:c.99C>A NP_006252.3:p.Thr33=
NM_006261.5:c.99C>A MANE Select NP_006252.4:p.Thr33=
Search 100 bp 5'
Search 100 bp 3'