Canonical Allele Identifier: CA564901099

Gene: PROP1

Linked Data

• dbSNP Id: rs781223542
• gnomAD v2: 5-177420059-G-C
• gnomAD v4: 5-177993058-G-C
• MyVariant Identifiers: chr5:g.177420059G>C (hg19) ; chr5:g.177993058G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177993058G>C , CM000667.2:g.177993058G>C	GRCh38
NC_000005.9:g.177420059G>C , CM000667.1:g.177420059G>C	GRCh37
NC_000005.8:g.177352665G>C	NCBI36
NG_015889.1:g.8185C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.343-11C>G MANE Select	ENSP00000311290.2:n.343-11C>G
NM_006261.4:c.343-11C>G	NP_006252.3:n.343-11C>G
NM_006261.5:c.343-11C>G MANE Select	NP_006252.4:n.343-11C>G