Canonical Allele Identifier: CA375769046
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140086728G>T (hg19) chr9:g.137192276G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192276G>T , CM000671.2:g.137192276G>T GRCh38
NC_000009.11:g.140086728G>T , CM000671.1:g.140086728G>T GRCh37
NC_000009.10:g.139206549G>T NCBI36
NG_027801.1:g.13436C>A
NG_027801.2:g.16918C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2056C>A MANE Select ENSP00000387100.4:p.Pro686Thr
ENST00000333046.8:c.1450C>A ENSP00000327617.4:p.Pro484Thr
ENST00000409012.4:c.2056C>A ENSP00000387100.4:p.Pro686Thr
ENST00000477345.1:n.2777C>A
NM_001128228.2:c.2056C>A NP_001121700.2:p.Pro686Thr
NM_001128228.3:c.2056C>A MANE Select NP_001121700.2:p.Pro686Thr
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