Canonical Allele Identifier: CA1603814049
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992934A= , CM000667.2:g.177992934A= GRCh38
NC_000005.9:g.177419935A= , CM000667.1:g.177419935A= GRCh37
NC_000005.8:g.177352541A= NCBI36
NG_015889.1:g.8309T=

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.456T= MANE Select ENSP00000311290.2:p.Ala152=
NM_006261.4:c.456T= NP_006252.3:p.Ala152=
NM_006261.5:c.456T= MANE Select NP_006252.4:p.Ala152=