Canonical Allele Identifier: CA1616428781
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1763408398

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278542del , CM000668.2:g.24278542del GRCh38
NC_000006.11:g.24278770del , CM000668.1:g.24278770del GRCh37
NC_000006.10:g.24386749del NCBI36
NG_012829.1:g.84511del
NG_012829.2:g.109751del

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.760-331del MANE Select ENSP00000367715.3:n.760-331del
ENST00000378454.7:c.760-331del ENSP00000367715.3:n.760-331del
NM_001195610.1:c.760-331del NP_001182539.1:n.760-331del
NM_016356.4:c.760-331del NP_057440.2:n.760-331del
NM_016356.5:c.760-331del MANE Select NP_057440.2:n.760-331del
NM_001195610.2:c.760-331del NP_001182539.1:n.760-331del