Canonical Allele Identifier: CA467925007

Gene: TPRN

Linked Data

• MyVariant Identifiers: chr9:g.140093895C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199443C>T , CM000671.2:g.137199443C>T	GRCh38
NC_000009.11:g.140093895C>T , CM000671.1:g.140093895C>T	GRCh37
NC_000009.10:g.139213716C>T	NCBI36
NG_027801.1:g.6269G>A
NG_027801.2:g.9751G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1269G>A MANE Select	ENSP00000387100.4:p.Leu423=
ENST00000333046.8:c.663G>A	ENSP00000327617.4:p.Leu221=
ENST00000409012.4:c.1269G>A	ENSP00000387100.4:p.Leu423=
ENST00000541945.1:n.90+4661G>A
NM_001128228.2:c.1269G>A	NP_001121700.2:p.Leu423=
NM_001128228.3:c.1269G>A MANE Select	NP_001121700.2:p.Leu423=