Canonical Allele Identifier: CA770955622

Gene: USP34

Linked Data

• dbSNP Id: rs1156949756
• MyVariant Identifiers: chr2:g.61605314_61605315insAG (hg19) ; chr2:g.61378179_61378180insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378182_61378183dup , CM000664.2:g.61378182_61378183dup	GRCh38
NC_000002.11:g.61605317_61605318dup , CM000664.1:g.61605317_61605318dup	GRCh37
NC_000002.10:g.61458821_61458822dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+182_1076+183dup MANE Select	ENSP00000381577.2:n.1076+182_1076+183dup
ENST00000398571.6:c.1076+182_1076+183dup	ENSP00000381577.2:n.1076+182_1076+183dup
ENST00000453133.1:c.602+182_602+183dup
NM_014709.3:c.1076+182_1076+183dup	NP_055524.3:n.1076+182_1076+183dup
NM_014709.4:c.1076+182_1076+183dup MANE Select	NP_055524.3:n.1076+182_1076+183dup