Canonical Allele Identifier: CA1884351143
Gene: TPRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199335A= , CM000671.2:g.137199335A= GRCh38
NC_000009.11:g.140093787A= , CM000671.1:g.140093787A= GRCh37
NC_000009.10:g.139213608A= NCBI36
NG_027801.1:g.6377T=
NG_027801.2:g.9859T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1377T= MANE Select ENSP00000387100.4:p.Asp459=
ENST00000333046.8:c.771T= ENSP00000327617.4:p.Asp257=
ENST00000409012.4:c.1377T= ENSP00000387100.4:p.Asp459=
ENST00000541945.1:n.90+4769T=
NM_001128228.2:c.1377T= NP_001121700.2:p.Asp459=
NM_001128228.3:c.1377T= MANE Select NP_001121700.2:p.Asp459=