Canonical Allele Identifier: CA1616324826
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24177860A= , CM000668.2:g.24177860A= GRCh38
NC_000006.11:g.24178088A= , CM000668.1:g.24178088A= GRCh37
NC_000006.10:g.24286067A= NCBI36
NG_012829.1:g.185193T=
NG_012829.2:g.210433T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1326+470T= MANE Select ENSP00000367715.3:n.1326+470T=
ENST00000378450.6:c.585+470T= ENSP00000367711.3:n.585+470T=
ENST00000378454.7:c.1326+470T= ENSP00000367715.3:n.1326+470T=
NM_001195610.1:c.1326+470T= NP_001182539.1:n.1326+470T=
NM_016356.4:c.1326+470T= NP_057440.2:n.1326+470T=
NM_016356.5:c.1326+470T= MANE Select NP_057440.2:n.1326+470T=
NM_001195610.2:c.1326+470T= NP_001182539.1:n.1326+470T=