Canonical Allele Identifier: CA132897378

Gene: PROP1

Linked Data

• dbSNP Id: rs904140644
• MyVariant Identifiers: chr5:g.177420029C>T (hg19) ; chr5:g.177993028C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177993028C>T , CM000667.2:g.177993028C>T	GRCh38
NC_000005.9:g.177420029C>T , CM000667.1:g.177420029C>T	GRCh37
NC_000005.8:g.177352635C>T	NCBI36
NG_015889.1:g.8215G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.362G>A MANE Select	ENSP00000311290.2:p.Arg121Lys
NM_006261.4:c.362G>A	NP_006252.3:p.Arg121Lys
NM_006261.5:c.362G>A MANE Select	NP_006252.4:p.Arg121Lys