Canonical Allele Identifier: CA426205633

Gene: USP34

Linked Data

• MyVariant Identifiers: chr2:g.61605574_61605576del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378441_61378443del , CM000664.2:g.61378441_61378443del	GRCh38
NC_000002.11:g.61605576_61605578del , CM000664.1:g.61605576_61605578del	GRCh37
NC_000002.10:g.61459080_61459082del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1015-17_1015-15del MANE Select	ENSP00000381577.2:n.1015-17_1015-15del
ENST00000398571.6:c.1015-17_1015-15del	ENSP00000381577.2:n.1015-17_1015-15del
ENST00000453133.1:c.541-17_541-15del
NM_014709.3:c.1015-17_1015-15del	NP_055524.3:n.1015-17_1015-15del
NM_014709.4:c.1015-17_1015-15del MANE Select	NP_055524.3:n.1015-17_1015-15del