Canonical Allele Identifier: CA2660167276
Gene: DUSP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143336del , CM000664.2:g.96143336del GRCh38
NC_000002.11:g.96809075del , CM000664.1:g.96809075del GRCh37
NC_000002.10:g.96172802del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*489del MANE Select ENSP00000288943.4:n.*489del
ENST00000288943.4:c.*489del ENSP00000288943.4:n.*489del
NM_004418.3:c.*489del NP_004409.1:n.*489del
XM_017003546.1:c.*489del XP_016859035.1:n.*489del
NM_004418.4:c.*489del MANE Select NP_004409.1:n.*489del