Canonical Allele Identifier: CA362379498

Gene: PROP1

Linked Data

• MyVariant Identifiers: chr5:g.177422869C>G (hg19) ; chr5:g.177995868C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177995868C>G , CM000667.2:g.177995868C>G	GRCh38
NC_000005.9:g.177422869C>G , CM000667.1:g.177422869C>G	GRCh37
NC_000005.8:g.177355475C>G	NCBI36
NG_015889.1:g.5375G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.66G>C MANE Select	ENSP00000311290.2:p.Leu22Phe
NM_006261.4:c.66G>C	NP_006252.3:p.Leu22Phe
NM_006261.5:c.66G>C MANE Select	NP_006252.4:p.Leu22Phe