Canonical Allele Identifier: CA1884347491
Gene: TPRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192277G= , CM000671.2:g.137192277G= GRCh38
NC_000009.11:g.140086729G= , CM000671.1:g.140086729G= GRCh37
NC_000009.10:g.139206550G= NCBI36
NG_027801.1:g.13435C=
NG_027801.2:g.16917C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2055C= MANE Select ENSP00000387100.4:p.Pro685=
ENST00000333046.8:c.1449C= ENSP00000327617.4:p.Pro483=
ENST00000409012.4:c.2055C= ENSP00000387100.4:p.Pro685=
ENST00000477345.1:n.2776C=
NM_001128228.2:c.2055C= NP_001121700.2:p.Pro685=
NM_001128228.3:c.2055C= MANE Select NP_001121700.2:p.Pro685=