Canonical Allele Identifier: CA1884351131
Gene: TPRN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199309_137199310delinsTG , CM000671.2:g.137199309_137199310delinsTG GRCh38
NC_000009.11:g.140093761_140093762delinsTG , CM000671.1:g.140093761_140093762delinsTG GRCh37
NC_000009.10:g.139213582_139213583delinsTG NCBI36
NG_027801.1:g.6402_6403delinsCA
NG_027801.2:g.9884_9885delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1402_1403delinsCA MANE Select ENSP00000387100.4:p.Gln468=
ENST00000333046.8:c.796_797delinsCA ENSP00000327617.4:p.Gln266=
ENST00000409012.4:c.1402_1403delinsCA ENSP00000387100.4:p.Gln468=
ENST00000541945.1:n.90+4794_90+4795delinsCA
NM_001128228.2:c.1402_1403delinsCA NP_001121700.2:p.Gln468=
NM_001128228.3:c.1402_1403delinsCA MANE Select NP_001121700.2:p.Gln468=
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