Canonical Allele Identifier: CA1603813911
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992657C= , CM000667.2:g.177992657C= GRCh38
NC_000005.9:g.177419658C= , CM000667.1:g.177419658C= GRCh37
NC_000005.8:g.177352264C= NCBI36
NG_015889.1:g.8586G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*52G= MANE Select ENSP00000311290.2:n.*52G=
NM_006261.4:c.*52G= NP_006252.3:n.*52G=
NM_006261.5:c.*52G= MANE Select NP_006252.4:n.*52G=