Canonical Allele Identifier: CA448355395
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177420004G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993003G>C , CM000667.2:g.177993003G>C GRCh38
NC_000005.9:g.177420004G>C , CM000667.1:g.177420004G>C GRCh37
NC_000005.8:g.177352610G>C NCBI36
NG_015889.1:g.8240C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.387C>G MANE Select ENSP00000311290.2:p.Arg129=
NM_006261.4:c.387C>G NP_006252.3:p.Arg129=
NM_006261.5:c.387C>G MANE Select NP_006252.4:p.Arg129=