Canonical Allele Identifier: CA1272472292
Gene: DUSP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143600G= , CM000664.2:g.96143600G= GRCh38
NC_000002.11:g.96809339G= , CM000664.1:g.96809339G= GRCh37
NC_000002.10:g.96173066G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*223C= MANE Select ENSP00000288943.4:n.*223C=
ENST00000288943.4:c.*223C= ENSP00000288943.4:n.*223C=
NM_004418.3:c.*223C= NP_004409.1:n.*223C=
XM_017003546.1:c.*223C= XP_016859035.1:n.*223C=
NM_004418.4:c.*223C= MANE Select NP_004409.1:n.*223C=
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