Canonical Allele Identifier: CA1616324801
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24177843T= , CM000668.2:g.24177843T= GRCh38
NC_000006.11:g.24178071T= , CM000668.1:g.24178071T= GRCh37
NC_000006.10:g.24286050T= NCBI36
NG_012829.1:g.185210A=
NG_012829.2:g.210450A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1326+487A= MANE Select ENSP00000367715.3:n.1326+487A=
ENST00000378450.6:c.585+487A= ENSP00000367711.3:n.585+487A=
ENST00000378454.7:c.1326+487A= ENSP00000367715.3:n.1326+487A=
NM_001195610.1:c.1326+487A= NP_001182539.1:n.1326+487A=
NM_016356.4:c.1326+487A= NP_057440.2:n.1326+487A=
NM_016356.5:c.1326+487A= MANE Select NP_057440.2:n.1326+487A=
NM_001195610.2:c.1326+487A= NP_001182539.1:n.1326+487A=