Canonical Allele Identifier: CA1616385989
Gene: DCDC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206671G= , CM000668.2:g.24206671G= GRCh38
NC_000006.11:g.24206899G= , CM000668.1:g.24206899G= GRCh37
NC_000006.10:g.24314878G= NCBI36
NG_012829.1:g.156382C=
NG_012829.2:g.181622C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.923-1569C= MANE Select ENSP00000367715.3:n.923-1569C=
ENST00000378454.7:c.923-1569C= ENSP00000367715.3:n.923-1569C=
NM_001195610.1:c.923-1569C= NP_001182539.1:n.923-1569C=
NM_016356.4:c.923-1569C= NP_057440.2:n.923-1569C=
NM_016356.5:c.923-1569C= MANE Select NP_057440.2:n.923-1569C=
NM_001195610.2:c.923-1569C= NP_001182539.1:n.923-1569C=
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