Canonical Allele Identifier: CA1616416900
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306139T= , CM000668.2:g.24306139T= GRCh38
NC_000006.11:g.24306367T= , CM000668.1:g.24306367T= GRCh37
NC_000006.10:g.24414346T= NCBI36
NG_012829.1:g.56914A=
NG_012829.2:g.82154A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-4095A= MANE Select ENSP00000367715.3:n.349-4095A=
ENST00000378454.7:c.349-4095A= ENSP00000367715.3:n.349-4095A=
NM_001195610.1:c.349-4095A= NP_001182539.1:n.349-4095A=
NM_016356.4:c.349-4095A= NP_057440.2:n.349-4095A=
NM_016356.5:c.349-4095A= MANE Select NP_057440.2:n.349-4095A=
NM_001195610.2:c.349-4095A= NP_001182539.1:n.349-4095A=