Canonical Allele Identifier: CA362378828
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177420003A>T (hg19) chr5:g.177993002A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993002A>T , CM000667.2:g.177993002A>T GRCh38
NC_000005.9:g.177420003A>T , CM000667.1:g.177420003A>T GRCh37
NC_000005.8:g.177352609A>T NCBI36
NG_015889.1:g.8241T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.388T>A MANE Select ENSP00000311290.2:p.Ser130Thr
NM_006261.4:c.388T>A NP_006252.3:p.Ser130Thr
NM_006261.5:c.388T>A MANE Select NP_006252.4:p.Ser130Thr
Search 100 bp 5'
Search 100 bp 3'