Canonical Allele Identifier: CA1033970275
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1682438721

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143365_96143372dup , CM000664.2:g.96143365_96143372dup GRCh38
NC_000002.11:g.96809104_96809111dup , CM000664.1:g.96809104_96809111dup GRCh37
NC_000002.10:g.96172831_96172838dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*452_*459dup MANE Select ENSP00000288943.4:n.*452_*459dup
ENST00000288943.4:c.*452_*459dup ENSP00000288943.4:n.*452_*459dup
NM_004418.3:c.*452_*459dup NP_004409.1:n.*452_*459dup
XM_017003546.1:c.*452_*459dup XP_016859035.1:n.*452_*459dup
NM_004418.4:c.*452_*459dup MANE Select NP_004409.1:n.*452_*459dup