Canonical Allele Identifier: CA2508554166
Gene: DUSP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143376C>T , CM000664.2:g.96143376C>T GRCh38
NC_000002.11:g.96809115C>T , CM000664.1:g.96809115C>T GRCh37
NC_000002.10:g.96172842C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*447G>A MANE Select ENSP00000288943.4:n.*447G>A
ENST00000288943.4:c.*447G>A ENSP00000288943.4:n.*447G>A
NM_004418.3:c.*447G>A NP_004409.1:n.*447G>A
XM_017003546.1:c.*447G>A XP_016859035.1:n.*447G>A
NM_004418.4:c.*447G>A MANE Select NP_004409.1:n.*447G>A
Search 100 bp 5'
Search 100 bp 3'