Canonical Allele Identifier: CA2581782258
Gene: DUSP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143592T>G , CM000664.2:g.96143592T>G GRCh38
NC_000002.11:g.96809331T>G , CM000664.1:g.96809331T>G GRCh37
NC_000002.10:g.96173058T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*231A>C MANE Select ENSP00000288943.4:n.*231A>C
ENST00000288943.4:c.*231A>C ENSP00000288943.4:n.*231A>C
NM_004418.3:c.*231A>C NP_004409.1:n.*231A>C
XM_017003546.1:c.*231A>C XP_016859035.1:n.*231A>C
NM_004418.4:c.*231A>C MANE Select NP_004409.1:n.*231A>C
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