Canonical Allele Identifier: CA2659222747
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378500-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378500G>C , CM000664.2:g.61378500G>C GRCh38
NC_000002.11:g.61605635G>C , CM000664.1:g.61605635G>C GRCh37
NC_000002.10:g.61459139G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-76C>G MANE Select ENSP00000381577.2:n.1015-76C>G
ENST00000398571.6:c.1015-76C>G ENSP00000381577.2:n.1015-76C>G
ENST00000453133.1:c.541-76C>G
NM_014709.3:c.1015-76C>G NP_055524.3:n.1015-76C>G
NM_014709.4:c.1015-76C>G MANE Select NP_055524.3:n.1015-76C>G