Canonical Allele Identifier: CA467852202
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140086735T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192283T>G , CM000671.2:g.137192283T>G GRCh38
NC_000009.11:g.140086735T>G , CM000671.1:g.140086735T>G GRCh37
NC_000009.10:g.139206556T>G NCBI36
NG_027801.1:g.13429A>C
NG_027801.2:g.16911A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2049A>C MANE Select ENSP00000387100.4:p.Ala683=
ENST00000333046.8:c.1443A>C ENSP00000327617.4:p.Ala481=
ENST00000409012.4:c.2049A>C ENSP00000387100.4:p.Ala683=
ENST00000477345.1:n.2770A>C
NM_001128228.2:c.2049A>C NP_001121700.2:p.Ala683=
NM_001128228.3:c.2049A>C MANE Select NP_001121700.2:p.Ala683=