Canonical Allele Identifier: CA362378888

Gene: PROP1

Linked Data

• gnomAD v4: 5-177993031-C-A
• MyVariant Identifiers: chr5:g.177420032C>A (hg19) ; chr5:g.177993031C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177993031C>A , CM000667.2:g.177993031C>A	GRCh38
NC_000005.9:g.177420032C>A , CM000667.1:g.177420032C>A	GRCh37
NC_000005.8:g.177352638C>A	NCBI36
NG_015889.1:g.8212G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.359G>T MANE Select	ENSP00000311290.2:p.Arg120Leu
NM_006261.4:c.359G>T	NP_006252.3:p.Arg120Leu
NM_006261.5:c.359G>T MANE Select	NP_006252.4:p.Arg120Leu