Canonical Allele Identifier: CA566222949
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1317113762
gnomAD v2: 6-24290802-ATTTGGT-A
gnomAD v3: 6-24290574-ATTTGGT-A
gnomAD v4: 6-24290574-ATTTGGT-A
MyVariant Identifiers: chr6:g.24290803_24290808del (hg19) chr6:g.24290575_24290580del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290575_24290580del , CM000668.2:g.24290575_24290580del GRCh38
NC_000006.11:g.24290803_24290808del , CM000668.1:g.24290803_24290808del GRCh37
NC_000006.10:g.24398782_24398787del NCBI36
NG_012829.1:g.72473_72478del
NG_012829.2:g.97713_97718del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+352_704+357del MANE Select ENSP00000367715.3:n.704+352_704+357del
ENST00000378454.7:c.704+352_704+357del ENSP00000367715.3:n.704+352_704+357del
NM_001195610.1:c.704+352_704+357del NP_001182539.1:n.704+352_704+357del
NM_016356.4:c.704+352_704+357del NP_057440.2:n.704+352_704+357del
NM_016356.5:c.704+352_704+357del MANE Select NP_057440.2:n.704+352_704+357del
NM_001195610.2:c.704+352_704+357del NP_001182539.1:n.704+352_704+357del
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