Canonical Allele Identifier: CA2677514149
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24174699-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174699G>T , CM000668.2:g.24174699G>T GRCh38
NC_000006.11:g.24174927G>T , CM000668.1:g.24174927G>T GRCh37
NC_000006.10:g.24282906G>T NCBI36
NG_012829.1:g.188354C>A
NG_012829.2:g.213594C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.*31C>A MANE Select ENSP00000367715.3:n.*31C>A
ENST00000378450.6:c.*31C>A ENSP00000367711.3:n.*31C>A
ENST00000378454.7:c.*31C>A ENSP00000367715.3:n.*31C>A
NM_001195610.1:c.*31C>A NP_001182539.1:n.*31C>A
NM_016356.4:c.*31C>A NP_057440.2:n.*31C>A
NM_016356.5:c.*31C>A MANE Select NP_057440.2:n.*31C>A
NM_001195610.2:c.*31C>A NP_001182539.1:n.*31C>A