Canonical Allele Identifier: CA1033970373
Gene: DUSP2 HGNC NCBI

Linked Data

gnomAD v3: 2-96143595-TTCC-T
gnomAD v4: 2-96143595-TTCC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143596_96143598del , CM000664.2:g.96143596_96143598del GRCh38
NC_000002.11:g.96809335_96809337del , CM000664.1:g.96809335_96809337del GRCh37
NC_000002.10:g.96173062_96173064del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*225_*227del MANE Select ENSP00000288943.4:n.*225_*227del
ENST00000288943.4:c.*225_*227del ENSP00000288943.4:n.*225_*227del
NM_004418.3:c.*225_*227del NP_004409.1:n.*225_*227del
XM_017003546.1:c.*225_*227del XP_016859035.1:n.*225_*227del
NM_004418.4:c.*225_*227del MANE Select NP_004409.1:n.*225_*227del
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Search 100 bp 3'