Canonical Allele Identifier: CA362378740
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3219054
ClinVar RCV Id: RCV004507408

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992957T>C , CM000667.2:g.177992957T>C GRCh38
NC_000005.9:g.177419958T>C , CM000667.1:g.177419958T>C GRCh37
NC_000005.8:g.177352564T>C NCBI36
NG_015889.1:g.8286A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.433A>G MANE Select ENSP00000311290.2:p.Ser145Gly
NM_006261.4:c.433A>G NP_006252.3:p.Ser145Gly
NM_006261.5:c.433A>G MANE Select NP_006252.4:p.Ser145Gly