Canonical Allele Identifier: CA1031337569

Gene: USP34

Linked Data

• dbSNP Id: rs1692852631
• gnomAD v3: 2-61378227-T-G
• gnomAD v4: 2-61378227-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378227T>G , CM000664.2:g.61378227T>G	GRCh38
NC_000002.11:g.61605362T>G , CM000664.1:g.61605362T>G	GRCh37
NC_000002.10:g.61458866T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+136A>C MANE Select	ENSP00000381577.2:n.1076+136A>C
ENST00000398571.6:c.1076+136A>C	ENSP00000381577.2:n.1076+136A>C
ENST00000453133.1:c.602+136A>C
NM_014709.3:c.1076+136A>C	NP_055524.3:n.1076+136A>C
NM_014709.4:c.1076+136A>C MANE Select	NP_055524.3:n.1076+136A>C