Canonical Allele Identifier: CA2659222596
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378236-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378236A>C , CM000664.2:g.61378236A>C GRCh38
NC_000002.11:g.61605371A>C , CM000664.1:g.61605371A>C GRCh37
NC_000002.10:g.61458875A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+127T>G MANE Select ENSP00000381577.2:n.1076+127T>G
ENST00000398571.6:c.1076+127T>G ENSP00000381577.2:n.1076+127T>G
ENST00000453133.1:c.602+127T>G
NM_014709.3:c.1076+127T>G NP_055524.3:n.1076+127T>G
NM_014709.4:c.1076+127T>G MANE Select NP_055524.3:n.1076+127T>G