Canonical Allele Identifier: CA362378726

Gene: PROP1

Linked Data

• MyVariant Identifiers: chr5:g.177419953G>C (hg19) ; chr5:g.177992952G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177992952G>C , CM000667.2:g.177992952G>C	GRCh38
NC_000005.9:g.177419953G>C , CM000667.1:g.177419953G>C	GRCh37
NC_000005.8:g.177352559G>C	NCBI36
NG_015889.1:g.8291C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.438C>G MANE Select	ENSP00000311290.2:p.Phe146Leu
NM_006261.4:c.438C>G	NP_006252.3:p.Phe146Leu
NM_006261.5:c.438C>G MANE Select	NP_006252.4:p.Phe146Leu