Canonical Allele Identifier: CA2660167201

Gene: DUSP2

Linked Data

• gnomAD v4: 2-96143269-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96143269A>C , CM000664.2:g.96143269A>C	GRCh38
NC_000002.11:g.96809008A>C , CM000664.1:g.96809008A>C	GRCh37
NC_000002.10:g.96172735A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288943.5:c.*554T>G MANE Select	ENSP00000288943.4:n.*554T>G
ENST00000288943.4:c.*554T>G	ENSP00000288943.4:n.*554T>G
NM_004418.3:c.*554T>G	NP_004409.1:n.*554T>G
XM_017003546.1:c.*554T>G	XP_016859035.1:n.*554T>G
NM_004418.4:c.*554T>G MANE Select	NP_004409.1:n.*554T>G