Canonical Allele Identifier: CA1603814222
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993353T= , CM000667.2:g.177993353T= GRCh38
NC_000005.9:g.177420354T= , CM000667.1:g.177420354T= GRCh37
NC_000005.8:g.177352960T= NCBI36
NG_015889.1:g.7890A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-306A= MANE Select ENSP00000311290.2:n.343-306A=
NM_006261.4:c.343-306A= NP_006252.3:n.343-306A=
NM_006261.5:c.343-306A= MANE Select NP_006252.4:n.343-306A=