Canonical Allele Identifier: CA375776046
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093753T>C (hg19) chr9:g.137199301T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199301T>C , CM000671.2:g.137199301T>C GRCh38
NC_000009.11:g.140093753T>C , CM000671.1:g.140093753T>C GRCh37
NC_000009.10:g.139213574T>C NCBI36
NG_027801.1:g.6411A>G
NG_027801.2:g.9893A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1411A>G MANE Select ENSP00000387100.4:p.Lys471Glu
ENST00000333046.8:c.805A>G ENSP00000327617.4:p.Lys269Glu
ENST00000409012.4:c.1411A>G ENSP00000387100.4:p.Lys471Glu
ENST00000541945.1:n.90+4803A>G
NM_001128228.2:c.1411A>G NP_001121700.2:p.Lys471Glu
NM_001128228.3:c.1411A>G MANE Select NP_001121700.2:p.Lys471Glu
Search 100 bp 5'
Search 100 bp 3'