Canonical Allele Identifier: CA2581782255
Gene: DUSP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143259G>C , CM000664.2:g.96143259G>C GRCh38
NC_000002.11:g.96808998G>C , CM000664.1:g.96808998G>C GRCh37
NC_000002.10:g.96172725G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*564C>G MANE Select ENSP00000288943.4:n.*564C>G
ENST00000288943.4:c.*564C>G ENSP00000288943.4:n.*564C>G
NM_004418.3:c.*564C>G NP_004409.1:n.*564C>G
XM_017003546.1:c.*564C>G XP_016859035.1:n.*564C>G
NM_004418.4:c.*564C>G MANE Select NP_004409.1:n.*564C>G