Canonical Allele Identifier: CA467853097
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093691T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199239T>C , CM000671.2:g.137199239T>C GRCh38
NC_000009.11:g.140093691T>C , CM000671.1:g.140093691T>C GRCh37
NC_000009.10:g.139213512T>C NCBI36
NG_027801.1:g.6473A>G
NG_027801.2:g.9955A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1473A>G MANE Select ENSP00000387100.4:p.Ala491=
ENST00000333046.8:c.867A>G ENSP00000327617.4:p.Ala289=
ENST00000409012.4:c.1473A>G ENSP00000387100.4:p.Ala491=
ENST00000541945.1:n.90+4865A>G
NM_001128228.2:c.1473A>G NP_001121700.2:p.Ala491=
NM_001128228.3:c.1473A>G MANE Select NP_001121700.2:p.Ala491=
Search 100 bp 5'
Search 100 bp 3'