Canonical Allele Identifier: CA2769598652
Gene: PROP1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993120G>C , CM000667.2:g.177993120G>C GRCh38
NC_000005.9:g.177420121G>C , CM000667.1:g.177420121G>C GRCh37
NC_000005.8:g.177352727G>C NCBI36
NG_015889.1:g.8123C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-73C>G MANE Select ENSP00000311290.2:n.343-73C>G
NM_006261.4:c.343-73C>G NP_006252.3:n.343-73C>G
NM_006261.5:c.343-73C>G MANE Select NP_006252.4:n.343-73C>G
Search 100 bp 5'
Search 100 bp 3'