Canonical Allele Identifier: CA136635991
Gene: DCDC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1276943
ClinVar RCV Id: RCV001690248
dbSNP Id: rs76420632
gnomAD v2: 6-24290925-T-TA
gnomAD v3: 6-24290697-T-TA
gnomAD v4: 6-24290697-T-TA
MyVariant Identifiers: chr6:g.24290926_24290927insA (hg19) chr6:g.24290925_24290926insA (hg19) chr6:g.24290698_24290699insA (hg38) chr6:g.24290697_24290698insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290706dup , CM000668.2:g.24290706dup GRCh38
NC_000006.11:g.24290934dup , CM000668.1:g.24290934dup GRCh37
NC_000006.10:g.24398913dup NCBI36
NG_012829.1:g.72355dup
NG_012829.2:g.97595dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.704+234dup MANE Select ENSP00000367715.3:n.704+234dup
ENST00000378454.7:c.704+234dup ENSP00000367715.3:n.704+234dup
NM_001195610.1:c.704+234dup NP_001182539.1:n.704+234dup
NM_016356.4:c.704+234dup NP_057440.2:n.704+234dup
NM_016356.5:c.704+234dup MANE Select NP_057440.2:n.704+234dup
NM_001195610.2:c.704+234dup NP_001182539.1:n.704+234dup
Search 100 bp 5'
Search 100 bp 3'