Canonical Allele Identifier: CA1272472168
Gene: DUSP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143319G= , CM000664.2:g.96143319G= GRCh38
NC_000002.11:g.96809058G= , CM000664.1:g.96809058G= GRCh37
NC_000002.10:g.96172785G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*504C= MANE Select ENSP00000288943.4:n.*504C=
ENST00000288943.4:c.*504C= ENSP00000288943.4:n.*504C=
NM_004418.3:c.*504C= NP_004409.1:n.*504C=
XM_017003546.1:c.*504C= XP_016859035.1:n.*504C=
NM_004418.4:c.*504C= MANE Select NP_004409.1:n.*504C=