Canonical Allele Identifier: CA2660167703

Gene: DUSP2

Linked Data

• gnomAD v4: 2-96143596-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96143599dup , CM000664.2:g.96143599dup	GRCh38
NC_000002.11:g.96809338dup , CM000664.1:g.96809338dup	GRCh37
NC_000002.10:g.96173065dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288943.5:c.*226dup MANE Select	ENSP00000288943.4:n.*226dup
ENST00000288943.4:c.*226dup	ENSP00000288943.4:n.*226dup
NM_004418.3:c.*226dup	NP_004409.1:n.*226dup
XM_017003546.1:c.*226dup	XP_016859035.1:n.*226dup
NM_004418.4:c.*226dup MANE Select	NP_004409.1:n.*226dup