Canonical Allele Identifier: CA1031337558

Gene: USP34

Linked Data

• dbSNP Id: rs1692851621
• gnomAD v3: 2-61378183-G-GA
• gnomAD v4: 2-61378183-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378183_61378184insA , CM000664.2:g.61378183_61378184insA	GRCh38
NC_000002.11:g.61605318_61605319insA , CM000664.1:g.61605318_61605319insA	GRCh37
NC_000002.10:g.61458822_61458823insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+179_1076+180insT MANE Select	ENSP00000381577.2:n.1076+179_1076+180insT
ENST00000398571.6:c.1076+179_1076+180insT	ENSP00000381577.2:n.1076+179_1076+180insT
ENST00000453133.1:c.602+179_602+180insT
NM_014709.3:c.1076+179_1076+180insT	NP_055524.3:n.1076+179_1076+180insT
NM_014709.4:c.1076+179_1076+180insT MANE Select	NP_055524.3:n.1076+179_1076+180insT