Canonical Allele Identifier: CA566222961
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs76420632
gnomAD v2: 6-24290925-T-TAA
gnomAD v3: 6-24290697-T-TAA
gnomAD v4: 6-24290697-T-TAA
MyVariant Identifiers: chr6:g.24290926_24290927insAA (hg19) chr6:g.24290925_24290926insAA (hg19) chr6:g.24290698_24290699insAA (hg38) chr6:g.24290697_24290698insAA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290705_24290706dup , CM000668.2:g.24290705_24290706dup GRCh38
NC_000006.11:g.24290933_24290934dup , CM000668.1:g.24290933_24290934dup GRCh37
NC_000006.10:g.24398912_24398913dup NCBI36
NG_012829.1:g.72354_72355dup
NG_012829.2:g.97594_97595dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+233_704+234dup MANE Select ENSP00000367715.3:n.704+233_704+234dup
ENST00000378454.7:c.704+233_704+234dup ENSP00000367715.3:n.704+233_704+234dup
NM_001195610.1:c.704+233_704+234dup NP_001182539.1:n.704+233_704+234dup
NM_016356.4:c.704+233_704+234dup NP_057440.2:n.704+233_704+234dup
NM_016356.5:c.704+233_704+234dup MANE Select NP_057440.2:n.704+233_704+234dup
NM_001195610.2:c.704+233_704+234dup NP_001182539.1:n.704+233_704+234dup
Search 100 bp 5'
Search 100 bp 3'