Canonical Allele Identifier: CA1603813988
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992799G= , CM000667.2:g.177992799G= GRCh38
NC_000005.9:g.177419800G= , CM000667.1:g.177419800G= GRCh37
NC_000005.8:g.177352406G= NCBI36
NG_015889.1:g.8444C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.591C= MANE Select ENSP00000311290.2:p.Thr197=
NM_006261.4:c.591C= NP_006252.3:p.Thr197=
NM_006261.5:c.591C= MANE Select NP_006252.4:p.Thr197=