Canonical Allele Identifier: CA1603813885
Gene: PROP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992588C= , CM000667.2:g.177992588C= GRCh38
NC_000005.9:g.177419589C= , CM000667.1:g.177419589C= GRCh37
NC_000005.8:g.177352195C= NCBI36
NG_015889.1:g.8655G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*121G= MANE Select ENSP00000311290.2:n.*121G=
NM_006261.4:c.*121G= NP_006252.3:n.*121G=
NM_006261.5:c.*121G= MANE Select NP_006252.4:n.*121G=
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