Canonical Allele Identifier: CA808117134

Gene: PROP1

Linked Data

• dbSNP Id: rs1483555602
• gnomAD v3: 5-177992675-G-T
• gnomAD v4: 5-177992675-G-T
• MyVariant Identifiers: chr5:g.177419676G>T (hg19) ; chr5:g.177992675G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177992675G>T , CM000667.2:g.177992675G>T	GRCh38
NC_000005.9:g.177419676G>T , CM000667.1:g.177419676G>T	GRCh37
NC_000005.8:g.177352282G>T	NCBI36
NG_015889.1:g.8568C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.*34C>A MANE Select	ENSP00000311290.2:n.*34C>A
NM_006261.4:c.*34C>A	NP_006252.3:n.*34C>A
NM_006261.5:c.*34C>A MANE Select	NP_006252.4:n.*34C>A