Canonical Allele Identifier: CA467924814

Gene: TPRN

Linked Data

• MyVariant Identifiers: chr9:g.140093781T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199329T>A , CM000671.2:g.137199329T>A	GRCh38
NC_000009.11:g.140093781T>A , CM000671.1:g.140093781T>A	GRCh37
NC_000009.10:g.139213602T>A	NCBI36
NG_027801.1:g.6383A>T
NG_027801.2:g.9865A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1383A>T MANE Select	ENSP00000387100.4:p.Val461=
ENST00000333046.8:c.777A>T	ENSP00000327617.4:p.Val259=
ENST00000409012.4:c.1383A>T	ENSP00000387100.4:p.Val461=
ENST00000541945.1:n.90+4775A>T
NM_001128228.2:c.1383A>T	NP_001121700.2:p.Val461=
NM_001128228.3:c.1383A>T MANE Select	NP_001121700.2:p.Val461=