Canonical Allele Identifier: CA2677514348
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24178282-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178283del , CM000668.2:g.24178283del GRCh38
NC_000006.11:g.24178511del , CM000668.1:g.24178511del GRCh37
NC_000006.10:g.24286490del NCBI36
NG_012829.1:g.184770del
NG_012829.2:g.210010del

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+47del MANE Select ENSP00000367715.3:n.1326+47del
ENST00000378450.6:c.585+47del ENSP00000367711.3:n.585+47del
ENST00000378454.7:c.1326+47del ENSP00000367715.3:n.1326+47del
NM_001195610.1:c.1326+47del NP_001182539.1:n.1326+47del
NM_016356.4:c.1326+47del NP_057440.2:n.1326+47del
NM_016356.5:c.1326+47del MANE Select NP_057440.2:n.1326+47del
NM_001195610.2:c.1326+47del NP_001182539.1:n.1326+47del
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