Canonical Allele Identifier: CA362378694
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992938G>C , CM000667.2:g.177992938G>C GRCh38
NC_000005.9:g.177419939G>C , CM000667.1:g.177419939G>C GRCh37
NC_000005.8:g.177352545G>C NCBI36
NG_015889.1:g.8305C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.452C>G MANE Select ENSP00000311290.2:p.Thr151Ser
NM_006261.4:c.452C>G NP_006252.3:p.Thr151Ser
NM_006261.5:c.452C>G MANE Select NP_006252.4:p.Thr151Ser