Canonical Allele Identifier: CA1031337550
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v3: 2-61378164-CCCTGTCT-C
gnomAD v4: 2-61378164-CCCTGTCT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378166_61378172del , CM000664.2:g.61378166_61378172del GRCh38
NC_000002.11:g.61605301_61605307del , CM000664.1:g.61605301_61605307del GRCh37
NC_000002.10:g.61458805_61458811del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+192_1076+198del MANE Select ENSP00000381577.2:n.1076+192_1076+198del
ENST00000398571.6:c.1076+192_1076+198del ENSP00000381577.2:n.1076+192_1076+198del
ENST00000453133.1:c.602+192_602+198del
NM_014709.3:c.1076+192_1076+198del NP_055524.3:n.1076+192_1076+198del
NM_014709.4:c.1076+192_1076+198del MANE Select NP_055524.3:n.1076+192_1076+198del
Search 100 bp 5'
Search 100 bp 3'