Canonical Allele Identifier: CA2659222658
Gene: USP34 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378298_61378303del , CM000664.2:g.61378298_61378303del GRCh38
NC_000002.11:g.61605433_61605438del , CM000664.1:g.61605433_61605438del GRCh37
NC_000002.10:g.61458937_61458942del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+60_1076+65del MANE Select ENSP00000381577.2:n.1076+60_1076+65del
ENST00000398571.6:c.1076+60_1076+65del ENSP00000381577.2:n.1076+60_1076+65del
ENST00000453133.1:c.602+60_602+65del
NM_014709.3:c.1076+60_1076+65del NP_055524.3:n.1076+60_1076+65del
NM_014709.4:c.1076+60_1076+65del MANE Select NP_055524.3:n.1076+60_1076+65del