Canonical Allele Identifier: CA1255352305
Gene: USP34 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378428T= , CM000664.2:g.61378428T= GRCh38
NC_000002.11:g.61605563T= , CM000664.1:g.61605563T= GRCh37
NC_000002.10:g.61459067T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-4A= MANE Select ENSP00000381577.2:n.1015-4A=
ENST00000398571.6:c.1015-4A= ENSP00000381577.2:n.1015-4A=
ENST00000453133.1:c.541-4A=
NM_014709.3:c.1015-4A= NP_055524.3:n.1015-4A=
NM_014709.4:c.1015-4A= MANE Select NP_055524.3:n.1015-4A=
Search 100 bp 5'
Search 100 bp 3'