Canonical Allele Identifier: CA467852919
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093658T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199206T>C , CM000671.2:g.137199206T>C GRCh38
NC_000009.11:g.140093658T>C , CM000671.1:g.140093658T>C GRCh37
NC_000009.10:g.139213479T>C NCBI36
NG_027801.1:g.6506A>G
NG_027801.2:g.9988A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1506A>G MANE Select ENSP00000387100.4:p.Thr502=
ENST00000333046.8:c.900A>G ENSP00000327617.4:p.Thr300=
ENST00000409012.4:c.1506A>G ENSP00000387100.4:p.Thr502=
ENST00000541945.1:n.90+4898A>G
NM_001128228.2:c.1506A>G NP_001121700.2:p.Thr502=
NM_001128228.3:c.1506A>G MANE Select NP_001121700.2:p.Thr502=
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