Canonical Allele Identifier: CA375776805
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093862C>A (hg19) chr9:g.137199410C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199410C>A , CM000671.2:g.137199410C>A GRCh38
NC_000009.11:g.140093862C>A , CM000671.1:g.140093862C>A GRCh37
NC_000009.10:g.139213683C>A NCBI36
NG_027801.1:g.6302G>T
NG_027801.2:g.9784G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1302G>T MANE Select ENSP00000387100.4:p.Glu434Asp
ENST00000333046.8:c.696G>T ENSP00000327617.4:p.Glu232Asp
ENST00000409012.4:c.1302G>T ENSP00000387100.4:p.Glu434Asp
ENST00000541945.1:n.90+4694G>T
NM_001128228.2:c.1302G>T NP_001121700.2:p.Glu434Asp
NM_001128228.3:c.1302G>T MANE Select NP_001121700.2:p.Glu434Asp
Search 100 bp 5'
Search 100 bp 3'