Canonical Allele Identifier: CA1272472171
Gene: DUSP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143327A= , CM000664.2:g.96143327A= GRCh38
NC_000002.11:g.96809066A= , CM000664.1:g.96809066A= GRCh37
NC_000002.10:g.96172793A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*496T= MANE Select ENSP00000288943.4:n.*496T=
ENST00000288943.4:c.*496T= ENSP00000288943.4:n.*496T=
NM_004418.3:c.*496T= NP_004409.1:n.*496T=
XM_017003546.1:c.*496T= XP_016859035.1:n.*496T=
NM_004418.4:c.*496T= MANE Select NP_004409.1:n.*496T=