Canonical Allele Identifier: CA1603814538
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177994156C= , CM000667.2:g.177994156C= GRCh38
NC_000005.9:g.177421157C= , CM000667.1:g.177421157C= GRCh37
NC_000005.8:g.177353763C= NCBI36
NG_015889.1:g.7087G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.292G= MANE Select ENSP00000311290.2:p.Ala98=
NM_006261.4:c.292G= NP_006252.3:p.Ala98=
NM_006261.5:c.292G= MANE Select NP_006252.4:p.Ala98=