Canonical Allele Identifier: CA1603813867
Gene: PROP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992542A= , CM000667.2:g.177992542A= GRCh38
NC_000005.9:g.177419543A= , CM000667.1:g.177419543A= GRCh37
NC_000005.8:g.177352149A= NCBI36
NG_015889.1:g.8701T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*167T= MANE Select ENSP00000311290.2:n.*167T=
NM_006261.4:c.*167T= NP_006252.3:n.*167T=
NM_006261.5:c.*167T= MANE Select NP_006252.4:n.*167T=