Canonical Allele Identifier: CA2660167710
Gene: DUSP2 HGNC NCBI

Linked Data

gnomAD v4: 2-96143599-CGACCCCGAATGAGGGCCAGCCTCAGTCCCCCAGCAGAAGAGCACCAGGTCGGAAAGACCAGCATGCCGGCATTCCTA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143602_96143678del , CM000664.2:g.96143602_96143678del GRCh38
NC_000002.11:g.96809341_96809417del , CM000664.1:g.96809341_96809417del GRCh37
NC_000002.10:g.96173068_96173144del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*147_*223del MANE Select ENSP00000288943.4:n.*147_*223del
ENST00000288943.4:c.*147_*223del ENSP00000288943.4:n.*147_*223del
NM_004418.3:c.*147_*223del NP_004409.1:n.*147_*223del
XM_017003546.1:c.*147_*223del XP_016859035.1:n.*147_*223del
NM_004418.4:c.*147_*223del MANE Select NP_004409.1:n.*147_*223del
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