Canonical Allele Identifier: CA375776928
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199428T>G , CM000671.2:g.137199428T>G GRCh38
NC_000009.11:g.140093880T>G , CM000671.1:g.140093880T>G GRCh37
NC_000009.10:g.139213701T>G NCBI36
NG_027801.1:g.6284A>C
NG_027801.2:g.9766A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1284A>C MANE Select ENSP00000387100.4:p.Glu428Asp
ENST00000333046.8:c.678A>C ENSP00000327617.4:p.Glu226Asp
ENST00000409012.4:c.1284A>C ENSP00000387100.4:p.Glu428Asp
ENST00000541945.1:n.90+4676A>C
NM_001128228.2:c.1284A>C NP_001121700.2:p.Glu428Asp
NM_001128228.3:c.1284A>C MANE Select NP_001121700.2:p.Glu428Asp