Canonical Allele Identifier: CA1603815332
Gene: PROP1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.95C= MANE Select ENSP00000311290.2:p.Pro32=
NM_006261.4:c.95C= NP_006252.3:p.Pro32=
NM_006261.5:c.95C= MANE Select NP_006252.4:p.Pro32=