Canonical Allele Identifier: CA1616406539
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760300361

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24348064del , CM000668.2:g.24348064del GRCh38
NC_000006.11:g.24348292del , CM000668.1:g.24348292del GRCh37
NC_000006.10:g.24456271del NCBI36
NG_012829.1:g.14991del
NG_012829.2:g.40231del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.348+5507del MANE Select ENSP00000367715.3:n.348+5507del
ENST00000378454.7:c.348+5507del ENSP00000367715.3:n.348+5507del
NM_001195610.1:c.348+5507del NP_001182539.1:n.348+5507del
NM_016356.4:c.348+5507del NP_057440.2:n.348+5507del
NM_016356.5:c.348+5507del MANE Select NP_057440.2:n.348+5507del
NM_001195610.2:c.348+5507del NP_001182539.1:n.348+5507del