Canonical Allele Identifier: CA375768129
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140086640G>C (hg19) chr9:g.137192188G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192188G>C , CM000671.2:g.137192188G>C GRCh38
NC_000009.11:g.140086640G>C , CM000671.1:g.140086640G>C GRCh37
NC_000009.10:g.139206461G>C NCBI36
NG_027801.1:g.13524C>G
NG_027801.2:g.17006C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2074-14C>G MANE Select ENSP00000387100.4:n.2074-14C>G
ENST00000333046.8:c.1538C>G ENSP00000327617.4:p.Ser513Cys
ENST00000409012.4:c.2074-14C>G ENSP00000387100.4:n.2074-14C>G
ENST00000477345.1:n.2795-14C>G
NM_001128228.2:c.2074-14C>G NP_001121700.2:n.2074-14C>G
NM_001128228.3:c.2074-14C>G MANE Select NP_001121700.2:n.2074-14C>G
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