Canonical Allele Identifier: CA1603815335
Gene: PROP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995843T= , CM000667.2:g.177995843T= GRCh38
NC_000005.9:g.177422844T= , CM000667.1:g.177422844T= GRCh37
NC_000005.8:g.177355450T= NCBI36
NG_015889.1:g.5400A=

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.91A= MANE Select ENSP00000311290.2:p.Thr31=
NM_006261.4:c.91A= NP_006252.3:p.Thr31=
NM_006261.5:c.91A= MANE Select NP_006252.4:p.Thr31=
Search 100 bp 5'
Search 100 bp 3'