Canonical Allele Identifier: CA2677514172
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24174788-G-GTAATTT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174790_24174795dup , CM000668.2:g.24174790_24174795dup GRCh38
NC_000006.11:g.24175018_24175023dup , CM000668.1:g.24175018_24175023dup GRCh37
NC_000006.10:g.24282997_24283002dup NCBI36
NG_012829.1:g.188259_188264dup
NG_012829.2:g.213499_213504dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1367_1372dup MANE Select ENSP00000367715.3:p.Ile457_Thr458insLysIle
ENST00000378450.6:c.626_631dup ENSP00000367711.3:p.Ile210_Thr211insLysIle
ENST00000378454.7:c.1367_1372dup ENSP00000367715.3:p.Ile457_Thr458insLysIle
NM_001195610.1:c.1367_1372dup NP_001182539.1:p.Ile457_Thr458insLysIle
NM_016356.4:c.1367_1372dup NP_057440.2:p.Ile457_Thr458insLysIle
NM_016356.5:c.1367_1372dup MANE Select NP_057440.2:p.Ile457_Thr458insLysIle
NM_001195610.2:c.1367_1372dup NP_001182539.1:p.Ile457_Thr458insLysIle
Search 100 bp 5'
Search 100 bp 3'