Canonical Allele Identifier: CA2576980468
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378493-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378493T>A , CM000664.2:g.61378493T>A GRCh38
NC_000002.11:g.61605628T>A , CM000664.1:g.61605628T>A GRCh37
NC_000002.10:g.61459132T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-69A>T MANE Select ENSP00000381577.2:n.1015-69A>T
ENST00000398571.6:c.1015-69A>T ENSP00000381577.2:n.1015-69A>T
ENST00000453133.1:c.541-69A>T
NM_014709.3:c.1015-69A>T NP_055524.3:n.1015-69A>T
NM_014709.4:c.1015-69A>T MANE Select NP_055524.3:n.1015-69A>T