Canonical Allele Identifier: CA467852205
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140086738C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192286C>T , CM000671.2:g.137192286C>T GRCh38
NC_000009.11:g.140086738C>T , CM000671.1:g.140086738C>T GRCh37
NC_000009.10:g.139206559C>T NCBI36
NG_027801.1:g.13426G>A
NG_027801.2:g.16908G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2046G>A MANE Select ENSP00000387100.4:p.Glu682=
ENST00000333046.8:c.1440G>A ENSP00000327617.4:p.Glu480=
ENST00000409012.4:c.2046G>A ENSP00000387100.4:p.Glu682=
ENST00000477345.1:n.2767G>A
NM_001128228.2:c.2046G>A NP_001121700.2:p.Glu682=
NM_001128228.3:c.2046G>A MANE Select NP_001121700.2:p.Glu682=