Canonical Allele Identifier: CA5362793
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs753551549

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199472G>A , CM000671.2:g.137199472G>A GRCh38
NC_000009.11:g.140093924G>A , CM000671.1:g.140093924G>A GRCh37
NC_000009.10:g.139213745G>A NCBI36
NG_027801.1:g.6240C>T
NG_027801.2:g.9722C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1240C>T MANE Select ENSP00000387100.4:p.Gln414Ter
ENST00000333046.8:c.634C>T ENSP00000327617.4:p.Gln212Ter
ENST00000409012.4:c.1240C>T ENSP00000387100.4:p.Gln414Ter
ENST00000541945.1:n.90+4632C>T
NM_001128228.2:c.1240C>T NP_001121700.2:p.Gln414Ter
NM_001128228.3:c.1240C>T MANE Select NP_001121700.2:p.Gln414Ter