Canonical Allele Identifier: CA2660167203
Gene: DUSP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143276del , CM000664.2:g.96143276del GRCh38
NC_000002.11:g.96809015del , CM000664.1:g.96809015del GRCh37
NC_000002.10:g.96172742del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*551del MANE Select ENSP00000288943.4:n.*551del
ENST00000288943.4:c.*551del ENSP00000288943.4:n.*551del
NM_004418.3:c.*551del NP_004409.1:n.*551del
XM_017003546.1:c.*551del XP_016859035.1:n.*551del
NM_004418.4:c.*551del MANE Select NP_004409.1:n.*551del