Canonical Allele Identifier: CA1677666

Gene: USP34

Linked Data

• dbSNP Id: rs150384375
• ExAC: 2:61605583 A / C
• gnomAD v2: 2-61605583-A-C
• gnomAD v3: 2-61378448-A-C
• gnomAD v4: 2-61378448-A-C
• MyVariant Identifiers: chr2:g.61605583A>C (hg19) ; chr2:g.61605583_61605584delinsCG (hg19) ; chr2:g.61378448A>C (hg38) ; chr2:g.61378448_61378449delinsCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378448A>C , CM000664.2:g.61378448A>C	GRCh38
NC_000002.11:g.61605583A>C , CM000664.1:g.61605583A>C	GRCh37
NC_000002.10:g.61459087A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1015-24T>G MANE Select	ENSP00000381577.2:n.1015-24T>G
ENST00000398571.6:c.1015-24T>G	ENSP00000381577.2:n.1015-24T>G
ENST00000453133.1:c.541-24T>G
NM_014709.3:c.1015-24T>G	NP_055524.3:n.1015-24T>G
NM_014709.4:c.1015-24T>G MANE Select	NP_055524.3:n.1015-24T>G