Canonical Allele Identifier: CA10581476
Gene: CDK13 HGNC NCBI

Linked Data

ClinVar Variation Id: 235887
ClinVar RCV Id: RCV000417211 RCV000498452 RCV000622786 RCV000850464 RCV001526523
dbSNP Id: rs878853160
MyVariant Identifiers: chr7:g.40085606A>G (hg19) chr7:g.40046007A>G (hg38)
PubMed: PMID:19344873 PMID:24999027 PMID:25560765 PMID:26539891 PMID:27479907 PMID:28135719 PMID:28807008 PMID:29021403 PMID:29222009
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40046007A>G , CM000669.2:g.40046007A>G GRCh38
NC_000007.13:g.40085606A>G , CM000669.1:g.40085606A>G GRCh37
NC_000007.12:g.40052131A>G NCBI36
NG_052965.1:g.100648A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000700485.1:n.261A>G
ENST00000700486.1:n.299A>G
ENST00000700487.1:n.267A>G
ENST00000181839.10:c.2525A>G MANE Select ENSP00000181839.4:p.Asn842Ser
ENST00000340829.10:c.2525A>G ENSP00000340557.5:p.Asn842Ser
ENST00000484589.2:c.1077A>G
ENST00000642592.1:c.78A>G
ENST00000643859.1:c.1416A>G
ENST00000643915.1:c.839A>G ENSP00000496187.1:p.Asn280Ser
ENST00000645470.1:c.455A>G ENSP00000495036.1:p.Asn152Ser
ENST00000646039.1:c.1865A>G ENSP00000494168.1:p.Asn622Ser
ENST00000647453.1:n.1594A>G
ENST00000181839.8:c.2525A>G ENSP00000181839.4:p.Asn842Ser
ENST00000340829.9:c.2525A>G ENSP00000340557.5:p.Asn842Ser
ENST00000484589.1:n.1077A>G
ENST00000611390.1:c.683A>G ENSP00000484610.1:p.Asn228Ser
ENST00000613626.4:c.683A>G ENSP00000480835.1:p.Asn228Ser
NM_003718.4:c.2525A>G NP_003709.3:p.Asn842Ser
NM_031267.3:c.2525A>G NP_112557.2:p.Asn842Ser
XM_011515597.1:c.2525A>G XP_011513899.1:p.Asn842Ser
XM_011515598.1:c.2525A>G XP_011513900.1:p.Asn842Ser
XM_011515597.3:c.2525A>G XP_011513899.1:p.Asn842Ser
XM_017012750.2:c.2525A>G XP_016868239.1:p.Asn842Ser
XM_017012751.2:c.2525A>G XP_016868240.1:p.Asn842Ser
NM_003718.5:c.2525A>G MANE Select NP_003709.3:p.Asn842Ser
Search 100 bp 5'
Search 100 bp 3'