Canonical Allele Identifier: CA2576980470
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378496-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378496C>T , CM000664.2:g.61378496C>T GRCh38
NC_000002.11:g.61605631C>T , CM000664.1:g.61605631C>T GRCh37
NC_000002.10:g.61459135C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-72G>A MANE Select ENSP00000381577.2:n.1015-72G>A
ENST00000398571.6:c.1015-72G>A ENSP00000381577.2:n.1015-72G>A
ENST00000453133.1:c.541-72G>A
NM_014709.3:c.1015-72G>A NP_055524.3:n.1015-72G>A
NM_014709.4:c.1015-72G>A MANE Select NP_055524.3:n.1015-72G>A