Canonical Allele Identifier: CA2769598654
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993146C>T , CM000667.2:g.177993146C>T GRCh38
NC_000005.9:g.177420147C>T , CM000667.1:g.177420147C>T GRCh37
NC_000005.8:g.177352753C>T NCBI36
NG_015889.1:g.8097G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-99G>A MANE Select ENSP00000311290.2:n.343-99G>A
NM_006261.4:c.343-99G>A NP_006252.3:n.343-99G>A
NM_006261.5:c.343-99G>A MANE Select NP_006252.4:n.343-99G>A