Canonical Allele Identifier: CA1603814009
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992854G= , CM000667.2:g.177992854G= GRCh38
NC_000005.9:g.177419855G= , CM000667.1:g.177419855G= GRCh37
NC_000005.8:g.177352461G= NCBI36
NG_015889.1:g.8389C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.536C= MANE Select ENSP00000311290.2:p.Pro179=
NM_006261.4:c.536C= NP_006252.3:p.Pro179=
NM_006261.5:c.536C= MANE Select NP_006252.4:p.Pro179=