Canonical Allele Identifier: CA2660167177
Gene: DUSP2 HGNC NCBI

Linked Data

gnomAD v4: 2-96143237-GTTTCCAACCCCTGCCCACAGGGCTAGGAGGAAGCGGGGGAGGGAGTGTTAAATGTCAGCTGAGCACAAATAAT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143244_96143316del , CM000664.2:g.96143244_96143316del GRCh38
NC_000002.11:g.96808983_96809055del , CM000664.1:g.96808983_96809055del GRCh37
NC_000002.10:g.96172710_96172782del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*513_*585del MANE Select ENSP00000288943.4:n.*513_*585del
ENST00000288943.4:c.*513_*585del ENSP00000288943.4:n.*513_*585del
NM_004418.3:c.*513_*585del NP_004409.1:n.*513_*585del
XM_017003546.1:c.*513_*585del XP_016859035.1:n.*513_*585del
NM_004418.4:c.*513_*585del MANE Select NP_004409.1:n.*513_*585del
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