Canonical Allele Identifier: CA375768062
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140086634T>G (hg19) chr9:g.137192182T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192182T>G , CM000671.2:g.137192182T>G GRCh38
NC_000009.11:g.140086634T>G , CM000671.1:g.140086634T>G GRCh37
NC_000009.10:g.139206455T>G NCBI36
NG_027801.1:g.13530A>C
NG_027801.2:g.17012A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2074-8A>C MANE Select ENSP00000387100.4:n.2074-8A>C
ENST00000333046.8:c.1544A>C ENSP00000327617.4:p.His515Pro
ENST00000409012.4:c.2074-8A>C ENSP00000387100.4:n.2074-8A>C
ENST00000477345.1:n.2795-8A>C
NM_001128228.2:c.2074-8A>C NP_001121700.2:n.2074-8A>C
NM_001128228.3:c.2074-8A>C MANE Select NP_001121700.2:n.2074-8A>C
Search 100 bp 5'
Search 100 bp 3'