Canonical Allele Identifier: CA1616321935
Gene: DCDC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174719T= , CM000668.2:g.24174719T= GRCh38
NC_000006.11:g.24174947T= , CM000668.1:g.24174947T= GRCh37
NC_000006.10:g.24282926T= NCBI36
NG_012829.1:g.188334A=
NG_012829.2:g.213574A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.*11A= MANE Select ENSP00000367715.3:n.*11A=
ENST00000378450.6:c.*11A= ENSP00000367711.3:n.*11A=
ENST00000378454.7:c.*11A= ENSP00000367715.3:n.*11A=
NM_001195610.1:c.*11A= NP_001182539.1:n.*11A=
NM_016356.4:c.*11A= NP_057440.2:n.*11A=
NM_016356.5:c.*11A= MANE Select NP_057440.2:n.*11A=
NM_001195610.2:c.*11A= NP_001182539.1:n.*11A=
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