Canonical Allele Identifier: CA983451148
Gene: DUSP14 HGNC NCBI

Linked Data

dbSNP Id: rs2054020128
gnomAD v3: 17-37490478-A-G
gnomAD v4: 17-37490478-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.37490478A>G , CM000679.2:g.37490478A>G GRCh38
NC_000017.10:g.35850584A>G , CM000679.1:g.35850584A>G GRCh37
NC_000017.9:g.32924697A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000617516.5:c.-181+520A>G MANE Select ENSP00000478595.1:n.-181+520A>G
ENST00000617516.4:c.-181+520A>G ENSP00000478595.1:n.-181+520A>G
NM_007026.3:c.-181+520A>G NP_008957.1:n.-181+520A>G
XM_011524234.1:c.-181+1523A>G XP_011522536.1:n.-181+1523A>G
XM_005256977.3:c.-1330A>G XP_005257034.1:n.-1330A>G
NM_007026.4:c.-181+520A>G MANE Select NP_008957.1:n.-181+520A>G
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