Canonical Allele Identifier: CA1255352340
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1692862739

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378482T>G , CM000664.2:g.61378482T>G GRCh38
NC_000002.11:g.61605617T>G , CM000664.1:g.61605617T>G GRCh37
NC_000002.10:g.61459121T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-58A>C MANE Select ENSP00000381577.2:n.1015-58A>C
ENST00000398571.6:c.1015-58A>C ENSP00000381577.2:n.1015-58A>C
ENST00000453133.1:c.541-58A>C
NM_014709.3:c.1015-58A>C NP_055524.3:n.1015-58A>C
NM_014709.4:c.1015-58A>C MANE Select NP_055524.3:n.1015-58A>C