Canonical Allele Identifier: CA2557560106

Gene: USP34

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378161A>G , CM000664.2:g.61378161A>G	GRCh38
NC_000002.11:g.61605296A>G , CM000664.1:g.61605296A>G	GRCh37
NC_000002.10:g.61458800A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+202T>C MANE Select	ENSP00000381577.2:n.1076+202T>C
ENST00000398571.6:c.1076+202T>C	ENSP00000381577.2:n.1076+202T>C
ENST00000453133.1:c.602+202T>C
NM_014709.3:c.1076+202T>C	NP_055524.3:n.1076+202T>C
NM_014709.4:c.1076+202T>C MANE Select	NP_055524.3:n.1076+202T>C