Canonical Allele Identifier: CA448346538
Gene: PROP1 HGNC NCBI

Linked Data

COSMIC: COSM3919770
MyVariant Identifiers: chr5:g.177419863A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992862A>T , CM000667.2:g.177992862A>T GRCh38
NC_000005.9:g.177419863A>T , CM000667.1:g.177419863A>T GRCh37
NC_000005.8:g.177352469A>T NCBI36
NG_015889.1:g.8381T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.528T>A MANE Select ENSP00000311290.2:p.Pro176=
NM_006261.4:c.528T>A NP_006252.3:p.Pro176=
NM_006261.5:c.528T>A MANE Select NP_006252.4:p.Pro176=
Search 100 bp 5'
Search 100 bp 3'