Canonical Allele Identifier: CA532842326

Gene: USP34

Linked Data

• dbSNP Id: rs955880080
• gnomAD v2: 2-61605307-C-CAAAAAAAAA
• MyVariant Identifiers: chr2:g.61605307_61605308insAAAAAAAAA (hg19) ; chr2:g.61378172_61378173insAAAAAAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378180_61378181insAAAAAAAAA , CM000664.2:g.61378180_61378181insAAAAAAAAA	GRCh38
NC_000002.11:g.61605315_61605316insAAAAAAAAA , CM000664.1:g.61605315_61605316insAAAAAAAAA	GRCh37
NC_000002.10:g.61458819_61458820insAAAAAAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+190_1076+191insTTTTTTTTT MANE Select	ENSP00000381577.2:n.1076+190_1076+191insTTTTTTTTT
ENST00000398571.6:c.1076+190_1076+191insTTTTTTTTT	ENSP00000381577.2:n.1076+190_1076+191insTTTTTTTTT
ENST00000453133.1:c.602+190_602+191insTTTTTTTTT
NM_014709.3:c.1076+190_1076+191insTTTTTTTTT	NP_055524.3:n.1076+190_1076+191insTTTTTTTTT
NM_014709.4:c.1076+190_1076+191insTTTTTTTTT MANE Select	NP_055524.3:n.1076+190_1076+191insTTTTTTTTT