Canonical Allele Identifier: CA2830535088
Gene: USP38 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143220167G>A , CM000666.2:g.143220167G>A GRCh38
NC_000004.11:g.144141320G>A , CM000666.1:g.144141320G>A GRCh37
NC_000004.10:g.144360770G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682469.1:c.2866-128G>A ENSP00000507210.1:n.2866-128G>A
ENST00000682486.1:n.1616-128G>A
ENST00000683224.1:c.*2141-128G>A ENSP00000508233.1:n.*2141-128G>A
ENST00000684586.1:c.2874-128G>A ENSP00000507201.1:n.2874-128G>A
ENST00000307017.9:c.2968-128G>A MANE Select ENSP00000303434.4:n.2968-128G>A
ENST00000307017.8:c.2968-128G>A ENSP00000303434.4:n.2968-128G>A
ENST00000511739.1:c.2841-128G>A ENSP00000424158.1:n.2841-128G>A
NM_001290326.1:c.1603-128G>A NP_001277255.1:n.1603-128G>A
NM_032557.6:c.2968-128G>A MANE Select NP_115946.2:n.2968-128G>A
XM_011532360.1:c.2866-128G>A XP_011530662.1:n.2866-128G>A
XM_011532360.3:c.2866-128G>A XP_011530662.1:n.2866-128G>A
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