Canonical Allele Identifier: CA2660167208
Gene: DUSP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143277del , CM000664.2:g.96143277del GRCh38
NC_000002.11:g.96809016del , CM000664.1:g.96809016del GRCh37
NC_000002.10:g.96172743del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*546del MANE Select ENSP00000288943.4:n.*546del
ENST00000288943.4:c.*546del ENSP00000288943.4:n.*546del
NM_004418.3:c.*546del NP_004409.1:n.*546del
XM_017003546.1:c.*546del XP_016859035.1:n.*546del
NM_004418.4:c.*546del MANE Select NP_004409.1:n.*546del