Canonical Allele Identifier: CA375769077
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs1834632719
MyVariant Identifiers: chr9:g.140086733T>C (hg19) chr9:g.137192281T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192281T>C , CM000671.2:g.137192281T>C GRCh38
NC_000009.11:g.140086733T>C , CM000671.1:g.140086733T>C GRCh37
NC_000009.10:g.139206554T>C NCBI36
NG_027801.1:g.13431A>G
NG_027801.2:g.16913A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.2051A>G MANE Select ENSP00000387100.4:p.Glu684Gly
ENST00000333046.8:c.1445A>G ENSP00000327617.4:p.Glu482Gly
ENST00000409012.4:c.2051A>G ENSP00000387100.4:p.Glu684Gly
ENST00000477345.1:n.2772A>G
NM_001128228.2:c.2051A>G NP_001121700.2:p.Glu684Gly
NM_001128228.3:c.2051A>G MANE Select NP_001121700.2:p.Glu684Gly
Search 100 bp 5'
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