Canonical Allele Identifier: CA1603813995
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992815T= , CM000667.2:g.177992815T= GRCh38
NC_000005.9:g.177419816T= , CM000667.1:g.177419816T= GRCh37
NC_000005.8:g.177352422T= NCBI36
NG_015889.1:g.8428A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.575A= MANE Select ENSP00000311290.2:p.Glu192=
NM_006261.4:c.575A= NP_006252.3:p.Glu192=
NM_006261.5:c.575A= MANE Select NP_006252.4:p.Glu192=