Canonical Allele Identifier: CA362379441
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177995839-G-C
MyVariant Identifiers: chr5:g.177422840G>C (hg19) chr5:g.177995839G>C (hg38)
PubMed: PMID:28263302
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995839G>C , CM000667.2:g.177995839G>C GRCh38
NC_000005.9:g.177422840G>C , CM000667.1:g.177422840G>C GRCh37
NC_000005.8:g.177355446G>C NCBI36
NG_015889.1:g.5404C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.95C>G MANE Select ENSP00000311290.2:p.Pro32Arg
NM_006261.4:c.95C>G NP_006252.3:p.Pro32Arg
NM_006261.5:c.95C>G MANE Select NP_006252.4:p.Pro32Arg
Search 100 bp 5'
Search 100 bp 3'