Canonical Allele Identifier: CA1255352168

Gene: USP34

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378172_61378174delinsCAA , CM000664.2:g.61378172_61378174delinsCAA	GRCh38
NC_000002.11:g.61605307_61605309delinsCAA , CM000664.1:g.61605307_61605309delinsCAA	GRCh37
NC_000002.10:g.61458811_61458813delinsCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+189_1076+191delinsTTG MANE Select	ENSP00000381577.2:n.1076+189_1076+191delinsTTG
ENST00000398571.6:c.1076+189_1076+191delinsTTG	ENSP00000381577.2:n.1076+189_1076+191delinsTTG
ENST00000453133.1:c.602+189_602+191delinsTTG
NM_014709.3:c.1076+189_1076+191delinsTTG	NP_055524.3:n.1076+189_1076+191delinsTTG
NM_014709.4:c.1076+189_1076+191delinsTTG MANE Select	NP_055524.3:n.1076+189_1076+191delinsTTG