Canonical Allele Identifier: CA375776684
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199388C>T , CM000671.2:g.137199388C>T GRCh38
NC_000009.11:g.140093840C>T , CM000671.1:g.140093840C>T GRCh37
NC_000009.10:g.139213661C>T NCBI36
NG_027801.1:g.6324G>A
NG_027801.2:g.9806G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1324G>A MANE Select ENSP00000387100.4:p.Ala442Thr
ENST00000333046.8:c.718G>A ENSP00000327617.4:p.Ala240Thr
ENST00000409012.4:c.1324G>A ENSP00000387100.4:p.Ala442Thr
ENST00000541945.1:n.90+4716G>A
NM_001128228.2:c.1324G>A NP_001121700.2:p.Ala442Thr
NM_001128228.3:c.1324G>A MANE Select NP_001121700.2:p.Ala442Thr