Canonical Allele Identifier: CA1603814092
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993032G= , CM000667.2:g.177993032G= GRCh38
NC_000005.9:g.177420033G= , CM000667.1:g.177420033G= GRCh37
NC_000005.8:g.177352639G= NCBI36
NG_015889.1:g.8211C=

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.358C= MANE Select ENSP00000311290.2:p.Arg120=
NM_006261.4:c.358C= NP_006252.3:p.Arg120=
NM_006261.5:c.358C= MANE Select NP_006252.4:p.Arg120=