Canonical Allele Identifier: CA467853146

Gene: TPRN

Linked Data

• MyVariant Identifiers: chr9:g.140093745G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199293G>T , CM000671.2:g.137199293G>T	GRCh38
NC_000009.11:g.140093745G>T , CM000671.1:g.140093745G>T	GRCh37
NC_000009.10:g.139213566G>T	NCBI36
NG_027801.1:g.6419C>A
NG_027801.2:g.9901C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1419C>A MANE Select	ENSP00000387100.4:p.Pro473=
ENST00000333046.8:c.813C>A	ENSP00000327617.4:p.Pro271=
ENST00000409012.4:c.1419C>A	ENSP00000387100.4:p.Pro473=
ENST00000541945.1:n.90+4811C>A
NM_001128228.2:c.1419C>A	NP_001121700.2:p.Pro473=
NM_001128228.3:c.1419C>A MANE Select	NP_001121700.2:p.Pro473=