Canonical Allele Identifier: CA1603814053
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992943C= , CM000667.2:g.177992943C= GRCh38
NC_000005.9:g.177419944C= , CM000667.1:g.177419944C= GRCh37
NC_000005.8:g.177352550C= NCBI36
NG_015889.1:g.8300G=

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.447G= MANE Select ENSP00000311290.2:p.Glu149=
NM_006261.4:c.447G= NP_006252.3:p.Glu149=
NM_006261.5:c.447G= MANE Select NP_006252.4:p.Glu149=