Canonical Allele Identifier: CA2659222731
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378484-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378484A>T , CM000664.2:g.61378484A>T GRCh38
NC_000002.11:g.61605619A>T , CM000664.1:g.61605619A>T GRCh37
NC_000002.10:g.61459123A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-60T>A MANE Select ENSP00000381577.2:n.1015-60T>A
ENST00000398571.6:c.1015-60T>A ENSP00000381577.2:n.1015-60T>A
ENST00000453133.1:c.541-60T>A
NM_014709.3:c.1015-60T>A NP_055524.3:n.1015-60T>A
NM_014709.4:c.1015-60T>A MANE Select NP_055524.3:n.1015-60T>A