Canonical Allele Identifier: CA770955640
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs1487766142
MyVariant Identifiers: chr2:g.61605345_61605347del (hg19) chr2:g.61378210_61378212del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378212_61378214del , CM000664.2:g.61378212_61378214del GRCh38
NC_000002.11:g.61605347_61605349del , CM000664.1:g.61605347_61605349del GRCh37
NC_000002.10:g.61458851_61458853del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+151_1076+153del MANE Select ENSP00000381577.2:n.1076+151_1076+153del
ENST00000398571.6:c.1076+151_1076+153del ENSP00000381577.2:n.1076+151_1076+153del
ENST00000453133.1:c.602+151_602+153del
NM_014709.3:c.1076+151_1076+153del NP_055524.3:n.1076+151_1076+153del
NM_014709.4:c.1076+151_1076+153del MANE Select NP_055524.3:n.1076+151_1076+153del
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