Canonical Allele Identifier: CA1255352169

Gene: USP34

Linked Data

• dbSNP Id: rs955880080

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378179_61378180del , CM000664.2:g.61378179_61378180del	GRCh38
NC_000002.11:g.61605314_61605315del , CM000664.1:g.61605314_61605315del	GRCh37
NC_000002.10:g.61458818_61458819del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+189_1076+190del MANE Select	ENSP00000381577.2:n.1076+189_1076+190del
ENST00000398571.6:c.1076+189_1076+190del	ENSP00000381577.2:n.1076+189_1076+190del
ENST00000453133.1:c.602+189_602+190del
NM_014709.3:c.1076+189_1076+190del	NP_055524.3:n.1076+189_1076+190del
NM_014709.4:c.1076+189_1076+190del MANE Select	NP_055524.3:n.1076+189_1076+190del