Canonical Allele Identifier: CA375768071
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140086637G>T (hg19) chr9:g.137192185G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192185G>T , CM000671.2:g.137192185G>T GRCh38
NC_000009.11:g.140086637G>T , CM000671.1:g.140086637G>T GRCh37
NC_000009.10:g.139206458G>T NCBI36
NG_027801.1:g.13527C>A
NG_027801.2:g.17009C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2074-11C>A MANE Select ENSP00000387100.4:n.2074-11C>A
ENST00000333046.8:c.1541C>A ENSP00000327617.4:p.Ser514Tyr
ENST00000409012.4:c.2074-11C>A ENSP00000387100.4:n.2074-11C>A
ENST00000477345.1:n.2795-11C>A
NM_001128228.2:c.2074-11C>A NP_001121700.2:n.2074-11C>A
NM_001128228.3:c.2074-11C>A MANE Select NP_001121700.2:n.2074-11C>A
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