Canonical Allele Identifier: CA362379060
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177421164G>T (hg19) chr5:g.177994163G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177994163G>T , CM000667.2:g.177994163G>T GRCh38
NC_000005.9:g.177421164G>T , CM000667.1:g.177421164G>T GRCh37
NC_000005.8:g.177353770G>T NCBI36
NG_015889.1:g.7080C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.285C>A MANE Select ENSP00000311290.2:p.Asp95Glu
NM_006261.4:c.285C>A NP_006252.3:p.Asp95Glu
NM_006261.5:c.285C>A MANE Select NP_006252.4:p.Asp95Glu
Search 100 bp 5'
Search 100 bp 3'