Canonical Allele Identifier: CA1603814129
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1582663267

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993121G>A , CM000667.2:g.177993121G>A GRCh38
NC_000005.9:g.177420122G>A , CM000667.1:g.177420122G>A GRCh37
NC_000005.8:g.177352728G>A NCBI36
NG_015889.1:g.8122C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-74C>T MANE Select ENSP00000311290.2:n.343-74C>T
NM_006261.4:c.343-74C>T NP_006252.3:n.343-74C>T
NM_006261.5:c.343-74C>T MANE Select NP_006252.4:n.343-74C>T