Canonical Allele Identifier: CA447990796
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177421155G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177994154G>T , CM000667.2:g.177994154G>T GRCh38
NC_000005.9:g.177421155G>T , CM000667.1:g.177421155G>T GRCh37
NC_000005.8:g.177353761G>T NCBI36
NG_015889.1:g.7089C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.294C>A MANE Select ENSP00000311290.2:p.Ala98=
NM_006261.4:c.294C>A NP_006252.3:p.Ala98=
NM_006261.5:c.294C>A MANE Select NP_006252.4:p.Ala98=