Canonical Allele Identifier: CA375769068
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140086732C>G (hg19) chr9:g.137192280C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192280C>G , CM000671.2:g.137192280C>G GRCh38
NC_000009.11:g.140086732C>G , CM000671.1:g.140086732C>G GRCh37
NC_000009.10:g.139206553C>G NCBI36
NG_027801.1:g.13432G>C
NG_027801.2:g.16914G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2052G>C MANE Select ENSP00000387100.4:p.Glu684Asp
ENST00000333046.8:c.1446G>C ENSP00000327617.4:p.Glu482Asp
ENST00000409012.4:c.2052G>C ENSP00000387100.4:p.Glu684Asp
ENST00000477345.1:n.2773G>C
NM_001128228.2:c.2052G>C NP_001121700.2:p.Glu684Asp
NM_001128228.3:c.2052G>C MANE Select NP_001121700.2:p.Glu684Asp
Search 100 bp 5'
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