Canonical Allele Identifier: CA2751310765
Gene: DUSP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143302A>C , CM000664.2:g.96143302A>C GRCh38
NC_000002.11:g.96809041A>C , CM000664.1:g.96809041A>C GRCh37
NC_000002.10:g.96172768A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*521T>G MANE Select ENSP00000288943.4:n.*521T>G
ENST00000288943.4:c.*521T>G ENSP00000288943.4:n.*521T>G
NM_004418.3:c.*521T>G NP_004409.1:n.*521T>G
XM_017003546.1:c.*521T>G XP_016859035.1:n.*521T>G
NM_004418.4:c.*521T>G MANE Select NP_004409.1:n.*521T>G