Canonical Allele Identifier: CA2660167694

Gene: DUSP2

Linked Data

• gnomAD v4: 2-96143590-CTTGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96143592_96143596del , CM000664.2:g.96143592_96143596del	GRCh38
NC_000002.11:g.96809331_96809335del , CM000664.1:g.96809331_96809335del	GRCh37
NC_000002.10:g.96173058_96173062del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288943.5:c.*228_*232del MANE Select	ENSP00000288943.4:n.*228_*232del
ENST00000288943.4:c.*228_*232del	ENSP00000288943.4:n.*228_*232del
NM_004418.3:c.*228_*232del	NP_004409.1:n.*228_*232del
XM_017003546.1:c.*228_*232del	XP_016859035.1:n.*228_*232del
NM_004418.4:c.*228_*232del MANE Select	NP_004409.1:n.*228_*232del