Canonical Allele Identifier: CA1616409139
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301666T= , CM000668.2:g.24301666T= GRCh38
NC_000006.11:g.24301894T= , CM000668.1:g.24301894T= GRCh37
NC_000006.10:g.24409873T= NCBI36
NG_012829.1:g.61387A=
NG_012829.2:g.86627A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.557+49A= MANE Select ENSP00000367715.3:n.557+49A=
ENST00000378454.7:c.557+49A= ENSP00000367715.3:n.557+49A=
NM_001195610.1:c.557+49A= NP_001182539.1:n.557+49A=
NM_016356.4:c.557+49A= NP_057440.2:n.557+49A=
NM_016356.5:c.557+49A= MANE Select NP_057440.2:n.557+49A=
NM_001195610.2:c.557+49A= NP_001182539.1:n.557+49A=