Canonical Allele Identifier: CA1616446169
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290447_24290450delinsATCC , CM000668.2:g.24290447_24290450delinsATCC GRCh38
NC_000006.11:g.24290675_24290678delinsATCC , CM000668.1:g.24290675_24290678delinsATCC GRCh37
NC_000006.10:g.24398654_24398657delinsATCC NCBI36
NG_012829.1:g.72603_72606delinsGGAT
NG_012829.2:g.97843_97846delinsGGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+482_704+485delinsGGAT MANE Select ENSP00000367715.3:n.704+482_704+485delinsGGAT
ENST00000378454.7:c.704+482_704+485delinsGGAT ENSP00000367715.3:n.704+482_704+485delinsGGAT
NM_001195610.1:c.704+482_704+485delinsGGAT NP_001182539.1:n.704+482_704+485delinsGGAT
NM_016356.4:c.704+482_704+485delinsGGAT NP_057440.2:n.704+482_704+485delinsGGAT
NM_016356.5:c.704+482_704+485delinsGGAT MANE Select NP_057440.2:n.704+482_704+485delinsGGAT
NM_001195610.2:c.704+482_704+485delinsGGAT NP_001182539.1:n.704+482_704+485delinsGGAT