Canonical Allele Identifier: CA2660167618

Gene: DUSP2

Linked Data

• gnomAD v4: 2-96143540-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96143540C>G , CM000664.2:g.96143540C>G	GRCh38
NC_000002.11:g.96809279C>G , CM000664.1:g.96809279C>G	GRCh37
NC_000002.10:g.96173006C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288943.5:c.*283G>C MANE Select	ENSP00000288943.4:n.*283G>C
ENST00000288943.4:c.*283G>C	ENSP00000288943.4:n.*283G>C
NM_004418.3:c.*283G>C	NP_004409.1:n.*283G>C
XM_017003546.1:c.*283G>C	XP_016859035.1:n.*283G>C
NM_004418.4:c.*283G>C MANE Select	NP_004409.1:n.*283G>C