Canonical Allele Identifier: CA1884351232
Gene: TPRN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199512G= , CM000671.2:g.137199512G= GRCh38
NC_000009.11:g.140093964G= , CM000671.1:g.140093964G= GRCh37
NC_000009.10:g.139213785G= NCBI36
NG_027801.1:g.6200C=
NG_027801.2:g.9682C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1200C= MANE Select ENSP00000387100.4:p.Pro400=
ENST00000333046.8:c.594C= ENSP00000327617.4:p.Pro198=
ENST00000409012.4:c.1200C= ENSP00000387100.4:p.Pro400=
ENST00000541945.1:n.90+4592C=
NM_001128228.2:c.1200C= NP_001121700.2:p.Pro400=
NM_001128228.3:c.1200C= MANE Select NP_001121700.2:p.Pro400=
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