Canonical Allele Identifier: CA375776668
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199385T>G , CM000671.2:g.137199385T>G GRCh38
NC_000009.11:g.140093837T>G , CM000671.1:g.140093837T>G GRCh37
NC_000009.10:g.139213658T>G NCBI36
NG_027801.1:g.6327A>C
NG_027801.2:g.9809A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.1327A>C MANE Select ENSP00000387100.4:p.Lys443Gln
ENST00000333046.8:c.721A>C ENSP00000327617.4:p.Lys241Gln
ENST00000409012.4:c.1327A>C ENSP00000387100.4:p.Lys443Gln
ENST00000541945.1:n.90+4719A>C
NM_001128228.2:c.1327A>C NP_001121700.2:p.Lys443Gln
NM_001128228.3:c.1327A>C MANE Select NP_001121700.2:p.Lys443Gln