Canonical Allele Identifier: CA448355431
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177420013C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993012C>T , CM000667.2:g.177993012C>T GRCh38
NC_000005.9:g.177420013C>T , CM000667.1:g.177420013C>T GRCh37
NC_000005.8:g.177352619C>T NCBI36
NG_015889.1:g.8231G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.378G>A MANE Select ENSP00000311290.2:p.Lys126=
NM_006261.4:c.378G>A NP_006252.3:p.Lys126=
NM_006261.5:c.378G>A MANE Select NP_006252.4:p.Lys126=