Canonical Allele Identifier: CA375775692
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199258G>T , CM000671.2:g.137199258G>T GRCh38
NC_000009.11:g.140093710G>T , CM000671.1:g.140093710G>T GRCh37
NC_000009.10:g.139213531G>T NCBI36
NG_027801.1:g.6454C>A
NG_027801.2:g.9936C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1454C>A MANE Select ENSP00000387100.4:p.Ala485Asp
ENST00000333046.8:c.848C>A ENSP00000327617.4:p.Ala283Asp
ENST00000409012.4:c.1454C>A ENSP00000387100.4:p.Ala485Asp
ENST00000541945.1:n.90+4846C>A
NM_001128228.2:c.1454C>A NP_001121700.2:p.Ala485Asp
NM_001128228.3:c.1454C>A MANE Select NP_001121700.2:p.Ala485Asp