Canonical Allele Identifier: CA2750154378

Gene: USP34

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378167T>C , CM000664.2:g.61378167T>C	GRCh38
NC_000002.11:g.61605302T>C , CM000664.1:g.61605302T>C	GRCh37
NC_000002.10:g.61458806T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+196A>G MANE Select	ENSP00000381577.2:n.1076+196A>G
ENST00000398571.6:c.1076+196A>G	ENSP00000381577.2:n.1076+196A>G
ENST00000453133.1:c.602+196A>G
NM_014709.3:c.1076+196A>G	NP_055524.3:n.1076+196A>G
NM_014709.4:c.1076+196A>G MANE Select	NP_055524.3:n.1076+196A>G