Canonical Allele Identifier: CA2016952798
Gene: DUSP16 HGNC NCBI

Linked Data

dbSNP Id: rs11612508

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12504579A>C , CM000674.2:g.12504579A>C GRCh38
NC_000012.11:g.12657513A>C , CM000674.1:g.12657513A>C GRCh37
NC_000012.10:g.12548780A>C NCBI36
NG_021402.1:g.62936T>G
NG_021402.2:g.62936T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298573.9:c.368-3897T>G MANE Select ENSP00000298573.5:n.368-3897T>G
ENST00000228862.3:c.367+15283T>G ENSP00000228862.3:n.367+15283T>G
ENST00000298573.8:c.368-3897T>G ENSP00000298573.5:n.368-3897T>G
ENST00000545864.1:n.100+1509T>G
NM_030640.2:c.368-3897T>G NP_085143.1:n.368-3897T>G
XM_005253488.1:c.87+15283T>G XP_005253545.1:n.87+15283T>G
XM_006719155.2:c.368-3897T>G XP_006719218.1:n.368-3897T>G
XM_011520856.1:c.368-3897T>G XP_011519158.1:n.368-3897T>G
XM_011520857.1:c.368-3897T>G XP_011519159.1:n.368-3897T>G
XM_005253488.3:c.87+15283T>G XP_005253545.1:n.87+15283T>G
XM_017019988.1:c.87+15283T>G XP_016875477.1:n.87+15283T>G
NM_030640.3:c.368-3897T>G MANE Select NP_085143.1:n.368-3897T>G