Canonical Allele Identifier: CA891862727
Gene: DCDC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 591519
ClinVar RCV Id: RCV000722698
dbSNP Id: rs1561878742
gnomAD v4: 6-24178474-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178475dup , CM000668.2:g.24178475dup GRCh38
NC_000006.11:g.24178703dup , CM000668.1:g.24178703dup GRCh37
NC_000006.10:g.24286682dup NCBI36
NG_012829.1:g.184578dup
NG_012829.2:g.209818dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1181dup MANE Select ENSP00000367715.3:p.His394GlnfsTer3
ENST00000378450.6:c.440dup ENSP00000367711.3:p.His147GlnfsTer3
ENST00000378454.7:c.1181dup ENSP00000367715.3:p.His394GlnfsTer3
NM_001195610.1:c.1181dup NP_001182539.1:p.His394GlnfsTer3
NM_016356.4:c.1181dup NP_057440.2:p.His394GlnfsTer3
NM_016356.5:c.1181dup MANE Select NP_057440.2:p.His394GlnfsTer3
NM_001195610.2:c.1181dup NP_001182539.1:p.His394GlnfsTer3
Search 100 bp 5'
Search 100 bp 3'