Canonical Allele Identifier: CA363280101
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs777259245

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178458G>T , CM000668.2:g.24178458G>T GRCh38
NC_000006.11:g.24178686G>T , CM000668.1:g.24178686G>T GRCh37
NC_000006.10:g.24286665G>T NCBI36
NG_012829.1:g.184595C>A
NG_012829.2:g.209835C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1198C>A MANE Select ENSP00000367715.3:p.Arg400Ser
ENST00000378450.6:c.457C>A ENSP00000367711.3:p.Arg153Ser
ENST00000378454.7:c.1198C>A ENSP00000367715.3:p.Arg400Ser
NM_001195610.1:c.1198C>A NP_001182539.1:p.Arg400Ser
NM_016356.4:c.1198C>A NP_057440.2:p.Arg400Ser
NM_016356.5:c.1198C>A MANE Select NP_057440.2:p.Arg400Ser
NM_001195610.2:c.1198C>A NP_001182539.1:p.Arg400Ser