Canonical Allele Identifier: CA1603815329
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995836G= , CM000667.2:g.177995836G= GRCh38
NC_000005.9:g.177422837G= , CM000667.1:g.177422837G= GRCh37
NC_000005.8:g.177355443G= NCBI36
NG_015889.1:g.5407C=

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.98C= MANE Select ENSP00000311290.2:p.Thr33=
NM_006261.4:c.98C= NP_006252.3:p.Thr33=
NM_006261.5:c.98C= MANE Select NP_006252.4:p.Thr33=