Canonical Allele Identifier: CA1616385100
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1761668543

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24204622_24204627del , CM000668.2:g.24204622_24204627del GRCh38
NC_000006.11:g.24204850_24204855del , CM000668.1:g.24204850_24204855del GRCh37
NC_000006.10:g.24312829_24312834del NCBI36
NG_012829.1:g.158428_158433del
NG_012829.2:g.183668_183673del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1023+377_1023+382del MANE Select ENSP00000367715.3:n.1023+377_1023+382del
ENST00000378450.6:c.282+377_282+382del ENSP00000367711.3:n.282+377_282+382del
ENST00000378454.7:c.1023+377_1023+382del ENSP00000367715.3:n.1023+377_1023+382del
NM_001195610.1:c.1023+377_1023+382del NP_001182539.1:n.1023+377_1023+382del
NM_016356.4:c.1023+377_1023+382del NP_057440.2:n.1023+377_1023+382del
NM_016356.5:c.1023+377_1023+382del MANE Select NP_057440.2:n.1023+377_1023+382del
NM_001195610.2:c.1023+377_1023+382del NP_001182539.1:n.1023+377_1023+382del