Canonical Allele Identifier: CA770956004

Gene: USP34

Linked Data

• dbSNP Id: rs1385408175
• MyVariant Identifiers: chr2:g.61605664_61605667del (hg19) ; chr2:g.61378529_61378532del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378531_61378534del , CM000664.2:g.61378531_61378534del	GRCh38
NC_000002.11:g.61605666_61605669del , CM000664.1:g.61605666_61605669del	GRCh37
NC_000002.10:g.61459170_61459173del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1015-108_1015-105del MANE Select	ENSP00000381577.2:n.1015-108_1015-105del
ENST00000398571.6:c.1015-108_1015-105del	ENSP00000381577.2:n.1015-108_1015-105del
ENST00000453133.1:c.541-108_541-105del
NM_014709.3:c.1015-108_1015-105del	NP_055524.3:n.1015-108_1015-105del
NM_014709.4:c.1015-108_1015-105del MANE Select	NP_055524.3:n.1015-108_1015-105del