Canonical Allele Identifier: CA2692798348

Gene: TPRN

Linked Data

• gnomAD v4: 9-137199315-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199317del , CM000671.2:g.137199317del	GRCh38
NC_000009.11:g.140093769del , CM000671.1:g.140093769del	GRCh37
NC_000009.10:g.139213590del	NCBI36
NG_027801.1:g.6396del
NG_027801.2:g.9878del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1396del MANE Select	ENSP00000387100.4:p.Ala466ProfsTer?
ENST00000333046.8:c.790del	ENSP00000327617.4:p.Ala264ProfsTer?
ENST00000409012.4:c.1396del	ENSP00000387100.4:p.Ala466ProfsTer?
ENST00000541945.1:n.90+4788del
NM_001128228.2:c.1396del	NP_001121700.2:p.Ala466ProfsTer?
NM_001128228.3:c.1396del MANE Select	NP_001121700.2:p.Ala466ProfsTer?