Canonical Allele Identifier: CA362379039
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177994155-G-T
MyVariant Identifiers: chr5:g.177421156G>T (hg19) chr5:g.177994155G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177994155G>T , CM000667.2:g.177994155G>T GRCh38
NC_000005.9:g.177421156G>T , CM000667.1:g.177421156G>T GRCh37
NC_000005.8:g.177353762G>T NCBI36
NG_015889.1:g.7088C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.293C>A MANE Select ENSP00000311290.2:p.Ala98Asp
NM_006261.4:c.293C>A NP_006252.3:p.Ala98Asp
NM_006261.5:c.293C>A MANE Select NP_006252.4:p.Ala98Asp
Search 100 bp 5'
Search 100 bp 3'