Canonical Allele Identifier: CA362378752
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992962A>T , CM000667.2:g.177992962A>T GRCh38
NC_000005.9:g.177419963A>T , CM000667.1:g.177419963A>T GRCh37
NC_000005.8:g.177352569A>T NCBI36
NG_015889.1:g.8281T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.428T>A MANE Select ENSP00000311290.2:p.Phe143Tyr
NM_006261.4:c.428T>A NP_006252.3:p.Phe143Tyr
NM_006261.5:c.428T>A MANE Select NP_006252.4:p.Phe143Tyr