Canonical Allele Identifier: CA375776657
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093836T>G (hg19) chr9:g.137199384T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199384T>G , CM000671.2:g.137199384T>G GRCh38
NC_000009.11:g.140093836T>G , CM000671.1:g.140093836T>G GRCh37
NC_000009.10:g.139213657T>G NCBI36
NG_027801.1:g.6328A>C
NG_027801.2:g.9810A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.1328A>C MANE Select ENSP00000387100.4:p.Lys443Thr
ENST00000333046.8:c.722A>C ENSP00000327617.4:p.Lys241Thr
ENST00000409012.4:c.1328A>C ENSP00000387100.4:p.Lys443Thr
ENST00000541945.1:n.90+4720A>C
NM_001128228.2:c.1328A>C NP_001121700.2:p.Lys443Thr
NM_001128228.3:c.1328A>C MANE Select NP_001121700.2:p.Lys443Thr
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