Canonical Allele Identifier: CA1603814056
Gene: PROP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992951A= , CM000667.2:g.177992951A= GRCh38
NC_000005.9:g.177419952A= , CM000667.1:g.177419952A= GRCh37
NC_000005.8:g.177352558A= NCBI36
NG_015889.1:g.8292T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.439T= MANE Select ENSP00000311290.2:p.Leu147=
NM_006261.4:c.439T= NP_006252.3:p.Leu147=
NM_006261.5:c.439T= MANE Select NP_006252.4:p.Leu147=
Search 100 bp 5'
Search 100 bp 3'