Canonical Allele Identifier: CA362378922
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993044A>T , CM000667.2:g.177993044A>T GRCh38
NC_000005.9:g.177420045A>T , CM000667.1:g.177420045A>T GRCh37
NC_000005.8:g.177352651A>T NCBI36
NG_015889.1:g.8199T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.346T>A MANE Select ENSP00000311290.2:p.Trp116Arg
NM_006261.4:c.346T>A NP_006252.3:p.Trp116Arg
NM_006261.5:c.346T>A MANE Select NP_006252.4:p.Trp116Arg