Canonical Allele Identifier: CA1616385119
Gene: DCDC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24204654G= , CM000668.2:g.24204654G= GRCh38
NC_000006.11:g.24204882G= , CM000668.1:g.24204882G= GRCh37
NC_000006.10:g.24312861G= NCBI36
NG_012829.1:g.158399C=
NG_012829.2:g.183639C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1023+348C= MANE Select ENSP00000367715.3:n.1023+348C=
ENST00000378450.6:c.282+348C= ENSP00000367711.3:n.282+348C=
ENST00000378454.7:c.1023+348C= ENSP00000367715.3:n.1023+348C=
NM_001195610.1:c.1023+348C= NP_001182539.1:n.1023+348C=
NM_016356.4:c.1023+348C= NP_057440.2:n.1023+348C=
NM_016356.5:c.1023+348C= MANE Select NP_057440.2:n.1023+348C=
NM_001195610.2:c.1023+348C= NP_001182539.1:n.1023+348C=
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