Canonical Allele Identifier: CA13682351

Gene: DUSP16

Linked Data

• dbSNP Id: rs11612508
• gnomAD v2: 12-12657513-A-G
• gnomAD v3: 12-12504579-A-G
• gnomAD v4: 12-12504579-A-G
• MyVariant Identifiers: chr12:g.12657513A>G (hg19) ; chr12:g.12504579A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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