Canonical Allele Identifier: CA1884351164
Gene: TPRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199373C= , CM000671.2:g.137199373C= GRCh38
NC_000009.11:g.140093825C= , CM000671.1:g.140093825C= GRCh37
NC_000009.10:g.139213646C= NCBI36
NG_027801.1:g.6339G=
NG_027801.2:g.9821G=

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.1339G= MANE Select ENSP00000387100.4:p.Glu447=
ENST00000333046.8:c.733G= ENSP00000327617.4:p.Glu245=
ENST00000409012.4:c.1339G= ENSP00000387100.4:p.Glu447=
ENST00000541945.1:n.90+4731G=
NM_001128228.2:c.1339G= NP_001121700.2:p.Glu447=
NM_001128228.3:c.1339G= MANE Select NP_001121700.2:p.Glu447=