Canonical Allele Identifier: CA363280083
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290935A>T , CM000668.2:g.24290935A>T GRCh38
NC_000006.11:g.24291163A>T , CM000668.1:g.24291163A>T GRCh37
NC_000006.10:g.24399142A>T NCBI36
NG_012829.1:g.72118T>A
NG_012829.2:g.97358T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.701T>A MANE Select ENSP00000367715.3:p.Phe234Tyr
ENST00000378454.7:c.701T>A ENSP00000367715.3:p.Phe234Tyr
NM_001195610.1:c.701T>A NP_001182539.1:p.Phe234Tyr
NM_016356.4:c.701T>A NP_057440.2:p.Phe234Tyr
NM_016356.5:c.701T>A MANE Select NP_057440.2:p.Phe234Tyr
NM_001195610.2:c.701T>A NP_001182539.1:p.Phe234Tyr