Canonical Allele Identifier: CA467852198
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs1411499852

Genomic Alleles

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

Transcript Alleles

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