Canonical Allele Identifier: CA1255352190

Gene: USP34

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378221_61378228delinsAAAGCTTC , CM000664.2:g.61378221_61378228delinsAAAGCTTC	GRCh38
NC_000002.11:g.61605356_61605363delinsAAAGCTTC , CM000664.1:g.61605356_61605363delinsAAAGCTTC	GRCh37
NC_000002.10:g.61458860_61458867delinsAAAGCTTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+135_1076+142delinsGAAGCTTT MANE Select	ENSP00000381577.2:n.1076+135_1076+142delinsGAAGCTTT
ENST00000398571.6:c.1076+135_1076+142delinsGAAGCTTT	ENSP00000381577.2:n.1076+135_1076+142delinsGAAGCTTT
ENST00000453133.1:c.602+135_602+142delinsGAAGCTTT
NM_014709.3:c.1076+135_1076+142delinsGAAGCTTT	NP_055524.3:n.1076+135_1076+142delinsGAAGCTTT
NM_014709.4:c.1076+135_1076+142delinsGAAGCTTT MANE Select	NP_055524.3:n.1076+135_1076+142delinsGAAGCTTT