Canonical Allele Identifier: CA983451160
Gene: DUSP14 HGNC NCBI

Linked Data

dbSNP Id: rs2054020455
gnomAD v3: 17-37490516-G-A
gnomAD v4: 17-37490516-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.37490516G>A , CM000679.2:g.37490516G>A GRCh38
NC_000017.10:g.35850622G>A , CM000679.1:g.35850622G>A GRCh37
NC_000017.9:g.32924735G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000617516.5:c.-181+558G>A MANE Select ENSP00000478595.1:n.-181+558G>A
ENST00000617516.4:c.-181+558G>A ENSP00000478595.1:n.-181+558G>A
NM_007026.3:c.-181+558G>A NP_008957.1:n.-181+558G>A
XM_011524234.1:c.-181+1561G>A XP_011522536.1:n.-181+1561G>A
XM_005256977.3:c.-1292G>A XP_005257034.1:n.-1292G>A
NM_007026.4:c.-181+558G>A MANE Select NP_008957.1:n.-181+558G>A
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