Canonical Allele Identifier: CA375776002
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199291T>A , CM000671.2:g.137199291T>A GRCh38
NC_000009.11:g.140093743T>A , CM000671.1:g.140093743T>A GRCh37
NC_000009.10:g.139213564T>A NCBI36
NG_027801.1:g.6421A>T
NG_027801.2:g.9903A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1421A>T MANE Select ENSP00000387100.4:p.Tyr474Phe
ENST00000333046.8:c.815A>T ENSP00000327617.4:p.Tyr272Phe
ENST00000409012.4:c.1421A>T ENSP00000387100.4:p.Tyr474Phe
ENST00000541945.1:n.90+4813A>T
NM_001128228.2:c.1421A>T NP_001121700.2:p.Tyr474Phe
NM_001128228.3:c.1421A>T MANE Select NP_001121700.2:p.Tyr474Phe