Canonical Allele Identifier: CA1086921835
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760966246

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178078_24178081del , CM000668.2:g.24178078_24178081del GRCh38
NC_000006.11:g.24178306_24178309del , CM000668.1:g.24178306_24178309del GRCh37
NC_000006.10:g.24286285_24286288del NCBI36
NG_012829.1:g.184972_184975del
NG_012829.2:g.210212_210215del

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+249_1326+252del MANE Select ENSP00000367715.3:n.1326+249_1326+252del
ENST00000378450.6:c.585+249_585+252del ENSP00000367711.3:n.585+249_585+252del
ENST00000378454.7:c.1326+249_1326+252del ENSP00000367715.3:n.1326+249_1326+252del
NM_001195610.1:c.1326+249_1326+252del NP_001182539.1:n.1326+249_1326+252del
NM_016356.4:c.1326+249_1326+252del NP_057440.2:n.1326+249_1326+252del
NM_016356.5:c.1326+249_1326+252del MANE Select NP_057440.2:n.1326+249_1326+252del
NM_001195610.2:c.1326+249_1326+252del NP_001182539.1:n.1326+249_1326+252del