Canonical Allele Identifier: CA362378497

Gene: PROP1

Linked Data

• gnomAD v4: 5-177992839-G-T
• MyVariant Identifiers: chr5:g.177419840G>T (hg19) ; chr5:g.177992839G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177992839G>T , CM000667.2:g.177992839G>T	GRCh38
NC_000005.9:g.177419840G>T , CM000667.1:g.177419840G>T	GRCh37
NC_000005.8:g.177352446G>T	NCBI36
NG_015889.1:g.8404C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.551C>A MANE Select	ENSP00000311290.2:p.Ala184Asp
NM_006261.4:c.551C>A	NP_006252.3:p.Ala184Asp
NM_006261.5:c.551C>A MANE Select	NP_006252.4:p.Ala184Asp