Canonical Allele Identifier: CA1603813862
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992515_177992516delinsCA , CM000667.2:g.177992515_177992516delinsCA GRCh38
NC_000005.9:g.177419516_177419517delinsCA , CM000667.1:g.177419516_177419517delinsCA GRCh37
NC_000005.8:g.177352122_177352123delinsCA NCBI36
NG_015889.1:g.8727_8728delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*193_*194delinsTG MANE Select ENSP00000311290.2:n.*193_*194delinsTG
NM_006261.4:c.*193_*194delinsTG NP_006252.3:n.*193_*194delinsTG
NM_006261.5:c.*193_*194delinsTG MANE Select NP_006252.4:n.*193_*194delinsTG