Canonical Allele Identifier: CA1603813892
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992599C= , CM000667.2:g.177992599C= GRCh38
NC_000005.9:g.177419600C= , CM000667.1:g.177419600C= GRCh37
NC_000005.8:g.177352206C= NCBI36
NG_015889.1:g.8644G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*110G= MANE Select ENSP00000311290.2:n.*110G=
NM_006261.4:c.*110G= NP_006252.3:n.*110G=
NM_006261.5:c.*110G= MANE Select NP_006252.4:n.*110G=