Canonical Allele Identifier: CA1603815331
Gene: PROP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995838C= , CM000667.2:g.177995838C= GRCh38
NC_000005.9:g.177422839C= , CM000667.1:g.177422839C= GRCh37
NC_000005.8:g.177355445C= NCBI36
NG_015889.1:g.5405G=

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.96G= MANE Select ENSP00000311290.2:p.Pro32=
NM_006261.4:c.96G= NP_006252.3:p.Pro32=
NM_006261.5:c.96G= MANE Select NP_006252.4:p.Pro32=
Search 100 bp 5'
Search 100 bp 3'