Canonical Allele Identifier: CA2711291839
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs2113738567

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178467_24178469dup , CM000668.2:g.24178467_24178469dup GRCh38
NC_000006.11:g.24178695_24178697dup , CM000668.1:g.24178695_24178697dup GRCh37
NC_000006.10:g.24286674_24286676dup NCBI36
NG_012829.1:g.184589_184591dup
NG_012829.2:g.209829_209831dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1192_1194dup MANE Select ENSP00000367715.3:p.Gln398_Ala399insGln
ENST00000378450.6:c.451_453dup ENSP00000367711.3:p.Gln151_Ala152insGln
ENST00000378454.7:c.1192_1194dup ENSP00000367715.3:p.Gln398_Ala399insGln
NM_001195610.1:c.1192_1194dup NP_001182539.1:p.Gln398_Ala399insGln
NM_016356.4:c.1192_1194dup NP_057440.2:p.Gln398_Ala399insGln
NM_016356.5:c.1192_1194dup MANE Select NP_057440.2:p.Gln398_Ala399insGln
NM_001195610.2:c.1192_1194dup NP_001182539.1:p.Gln398_Ala399insGln