Canonical Allele Identifier: CA1031337552

Gene: USP34

Linked Data

• gnomAD v3: 2-61378172-C-CAAAAAAA
• gnomAD v4: 2-61378172-C-CAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378174_61378180dup , CM000664.2:g.61378174_61378180dup	GRCh38
NC_000002.11:g.61605309_61605315dup , CM000664.1:g.61605309_61605315dup	GRCh37
NC_000002.10:g.61458813_61458819dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+184_1076+190dup MANE Select	ENSP00000381577.2:n.1076+184_1076+190dup
ENST00000398571.6:c.1076+184_1076+190dup	ENSP00000381577.2:n.1076+184_1076+190dup
ENST00000453133.1:c.602+184_602+190dup
NM_014709.3:c.1076+184_1076+190dup	NP_055524.3:n.1076+184_1076+190dup
NM_014709.4:c.1076+184_1076+190dup MANE Select	NP_055524.3:n.1076+184_1076+190dup