Canonical Allele Identifier: CA1616410437
Gene: DCDC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24302183T= , CM000668.2:g.24302183T= GRCh38
NC_000006.11:g.24302411T= , CM000668.1:g.24302411T= GRCh37
NC_000006.10:g.24410390T= NCBI36
NG_012829.1:g.60870A=
NG_012829.2:g.86110A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-139A= MANE Select ENSP00000367715.3:n.349-139A=
ENST00000378454.7:c.349-139A= ENSP00000367715.3:n.349-139A=
NM_001195610.1:c.349-139A= NP_001182539.1:n.349-139A=
NM_016356.4:c.349-139A= NP_057440.2:n.349-139A=
NM_016356.5:c.349-139A= MANE Select NP_057440.2:n.349-139A=
NM_001195610.2:c.349-139A= NP_001182539.1:n.349-139A=
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