Canonical Allele Identifier: CA375776824
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093864C>G (hg19) chr9:g.137199412C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199412C>G , CM000671.2:g.137199412C>G GRCh38
NC_000009.11:g.140093864C>G , CM000671.1:g.140093864C>G GRCh37
NC_000009.10:g.139213685C>G NCBI36
NG_027801.1:g.6300G>C
NG_027801.2:g.9782G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1300G>C MANE Select ENSP00000387100.4:p.Glu434Gln
ENST00000333046.8:c.694G>C ENSP00000327617.4:p.Glu232Gln
ENST00000409012.4:c.1300G>C ENSP00000387100.4:p.Glu434Gln
ENST00000541945.1:n.90+4692G>C
NM_001128228.2:c.1300G>C NP_001121700.2:p.Glu434Gln
NM_001128228.3:c.1300G>C MANE Select NP_001121700.2:p.Glu434Gln
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