Canonical Allele Identifier: CA591373023
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs772232586

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199267_137199284dup , CM000671.2:g.137199267_137199284dup GRCh38
NC_000009.11:g.140093719_140093736dup , CM000671.1:g.140093719_140093736dup GRCh37
NC_000009.10:g.139213540_139213557dup NCBI36
NG_027801.1:g.6443_6460dup
NG_027801.2:g.9925_9942dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1443_1460dup MANE Select ENSP00000387100.4:p.Pro487_Gly488insLeuHisProAlaArgPro
ENST00000333046.8:c.837_854dup ENSP00000327617.4:p.Pro285_Gly286insLeuHisProAlaArgPro
ENST00000409012.4:c.1443_1460dup ENSP00000387100.4:p.Pro487_Gly488insLeuHisProAlaArgPro
ENST00000541945.1:n.90+4835_90+4852dup
NM_001128228.2:c.1443_1460dup NP_001121700.2:p.Pro487_Gly488insLeuHisProAlaArgPro
NM_001128228.3:c.1443_1460dup MANE Select NP_001121700.2:p.Pro487_Gly488insLeuHisProAlaArgPro