Canonical Allele Identifier: CA363278533
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24174741-C-T
COSMIC: COSM266348

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174741C>T , CM000668.2:g.24174741C>T GRCh38
NC_000006.11:g.24174969C>T , CM000668.1:g.24174969C>T GRCh37
NC_000006.10:g.24282948C>T NCBI36
NG_012829.1:g.188312G>A
NG_012829.2:g.213552G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1420G>A MANE Select ENSP00000367715.3:p.Ala474Thr
ENST00000378450.6:c.679G>A ENSP00000367711.3:p.Ala227Thr
ENST00000378454.7:c.1420G>A ENSP00000367715.3:p.Ala474Thr
NM_001195610.1:c.1420G>A NP_001182539.1:p.Ala474Thr
NM_016356.4:c.1420G>A NP_057440.2:p.Ala474Thr
NM_016356.5:c.1420G>A MANE Select NP_057440.2:p.Ala474Thr
NM_001195610.2:c.1420G>A NP_001182539.1:p.Ala474Thr