Canonical Allele Identifier: CA362379512

Gene: PROP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177995875T>A , CM000667.2:g.177995875T>A	GRCh38
NC_000005.9:g.177422876T>A , CM000667.1:g.177422876T>A	GRCh37
NC_000005.8:g.177355482T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.59A>T MANE Select	ENSP00000311290.2:p.Asn20Ile
NM_006261.5:c.59A>T MANE Select	NP_006252.4:p.Asn20Ile