Canonical Allele Identifier: CA566222959
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs76420632
gnomAD v2: 6-24290925-TA-T
gnomAD v3: 6-24290697-TA-T
gnomAD v4: 6-24290697-TA-T
COSMIC: COSN23258505
MyVariant Identifiers: chr6:g.24290926del (hg19) chr6:g.24290698del (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+234del MANE Select ENSP00000367715.3:n.704+234del
ENST00000378454.7:c.704+234del ENSP00000367715.3:n.704+234del
NM_001195610.1:c.704+234del NP_001182539.1:n.704+234del
NM_016356.4:c.704+234del NP_057440.2:n.704+234del
NM_016356.5:c.704+234del MANE Select NP_057440.2:n.704+234del
NM_001195610.2:c.704+234del NP_001182539.1:n.704+234del
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