Canonical Allele Identifier: CA2692798386

Gene: TPRN

Linked Data

• gnomAD v4: 9-137199324-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199325dup , CM000671.2:g.137199325dup	GRCh38
NC_000009.11:g.140093777dup , CM000671.1:g.140093777dup	GRCh37
NC_000009.10:g.139213598dup	NCBI36
NG_027801.1:g.6387dup
NG_027801.2:g.9869dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1387dup MANE Select	ENSP00000387100.4:p.Ser463PhefsTer?
ENST00000333046.8:c.781dup	ENSP00000327617.4:p.Ser261PhefsTer?
ENST00000409012.4:c.1387dup	ENSP00000387100.4:p.Ser463PhefsTer?
ENST00000541945.1:n.90+4779dup
NM_001128228.2:c.1387dup	NP_001121700.2:p.Ser463PhefsTer?
NM_001128228.3:c.1387dup MANE Select	NP_001121700.2:p.Ser463PhefsTer?