Canonical Allele Identifier: CA1603815334
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995842G= , CM000667.2:g.177995842G= GRCh38
NC_000005.9:g.177422843G= , CM000667.1:g.177422843G= GRCh37
NC_000005.8:g.177355449G= NCBI36
NG_015889.1:g.5401C=

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.92C= MANE Select ENSP00000311290.2:p.Thr31=
NM_006261.4:c.92C= NP_006252.3:p.Thr31=
NM_006261.5:c.92C= MANE Select NP_006252.4:p.Thr31=