Canonical Allele Identifier: CA375769054
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192279G>T , CM000671.2:g.137192279G>T GRCh38
NC_000009.11:g.140086731G>T , CM000671.1:g.140086731G>T GRCh37
NC_000009.10:g.139206552G>T NCBI36
NG_027801.1:g.13433C>A
NG_027801.2:g.16915C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2053C>A MANE Select ENSP00000387100.4:p.Pro685Thr
ENST00000333046.8:c.1447C>A ENSP00000327617.4:p.Pro483Thr
ENST00000409012.4:c.2053C>A ENSP00000387100.4:p.Pro685Thr
ENST00000477345.1:n.2774C>A
NM_001128228.2:c.2053C>A NP_001121700.2:p.Pro685Thr
NM_001128228.3:c.2053C>A MANE Select NP_001121700.2:p.Pro685Thr