Canonical Allele Identifier: CA532842324

Gene: USP34

Linked Data

• gnomAD v2: 2-61605298-ACCCTGTCTC-A
• MyVariant Identifiers: chr2:g.61605299_61605307del (hg19) ; chr2:g.61378164_61378172del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378164_61378172del , CM000664.2:g.61378164_61378172del	GRCh38
NC_000002.11:g.61605299_61605307del , CM000664.1:g.61605299_61605307del	GRCh37
NC_000002.10:g.61458803_61458811del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+191_1076+199del MANE Select	ENSP00000381577.2:n.1076+191_1076+199del
ENST00000398571.6:c.1076+191_1076+199del	ENSP00000381577.2:n.1076+191_1076+199del
ENST00000453133.1:c.602+191_602+199del
NM_014709.3:c.1076+191_1076+199del	NP_055524.3:n.1076+191_1076+199del
NM_014709.4:c.1076+191_1076+199del MANE Select	NP_055524.3:n.1076+191_1076+199del