Canonical Allele Identifier: CA362378599
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992889G>T , CM000667.2:g.177992889G>T GRCh38
NC_000005.9:g.177419890G>T , CM000667.1:g.177419890G>T GRCh37
NC_000005.8:g.177352496G>T NCBI36
NG_015889.1:g.8354C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.501C>A MANE Select ENSP00000311290.2:p.Phe167Leu
NM_006261.4:c.501C>A NP_006252.3:p.Phe167Leu
NM_006261.5:c.501C>A MANE Select NP_006252.4:p.Phe167Leu