Canonical Allele Identifier: CA1603814123
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993100_177993101delinsAC , CM000667.2:g.177993100_177993101delinsAC GRCh38
NC_000005.9:g.177420101_177420102delinsAC , CM000667.1:g.177420101_177420102delinsAC GRCh37
NC_000005.8:g.177352707_177352708delinsAC NCBI36
NG_015889.1:g.8142_8143delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-54_343-53delinsGT MANE Select ENSP00000311290.2:n.343-54_343-53delinsGT
NM_006261.4:c.343-54_343-53delinsGT NP_006252.3:n.343-54_343-53delinsGT
NM_006261.5:c.343-54_343-53delinsGT MANE Select NP_006252.4:n.343-54_343-53delinsGT