Canonical Allele Identifier: CA467853162
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs1834757335
MyVariant Identifiers: chr9:g.140093769C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199317C>T , CM000671.2:g.137199317C>T GRCh38
NC_000009.11:g.140093769C>T , CM000671.1:g.140093769C>T GRCh37
NC_000009.10:g.139213590C>T NCBI36
NG_027801.1:g.6395G>A
NG_027801.2:g.9877G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1395G>A MANE Select ENSP00000387100.4:p.Glu465=
ENST00000333046.8:c.789G>A ENSP00000327617.4:p.Glu263=
ENST00000409012.4:c.1395G>A ENSP00000387100.4:p.Glu465=
ENST00000541945.1:n.90+4787G>A
NM_001128228.2:c.1395G>A NP_001121700.2:p.Glu465=
NM_001128228.3:c.1395G>A MANE Select NP_001121700.2:p.Glu465=