Canonical Allele Identifier: CA2676775199
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993058dup , CM000667.2:g.177993058dup GRCh38
NC_000005.9:g.177420059dup , CM000667.1:g.177420059dup GRCh37
NC_000005.8:g.177352665dup NCBI36
NG_015889.1:g.8188dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-8dup MANE Select ENSP00000311290.2:n.343-8dup
NM_006261.4:c.343-8dup NP_006252.3:n.343-8dup
NM_006261.5:c.343-8dup MANE Select NP_006252.4:n.343-8dup