Canonical Allele Identifier: CA566224230

Gene: DCDC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24347816del , CM000668.2:g.24347816del	GRCh38
NC_000006.11:g.24348044del , CM000668.1:g.24348044del	GRCh37
NC_000006.10:g.24456023del	NCBI36
NG_012829.1:g.15239del
NG_012829.2:g.40479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.348+5755del MANE Select	ENSP00000367715.3:n.348+5755del
ENST00000378454.7:c.348+5755del	ENSP00000367715.3:n.348+5755del
NM_001195610.1:c.348+5755del	NP_001182539.1:n.348+5755del
NM_016356.4:c.348+5755del	NP_057440.2:n.348+5755del
NM_016356.5:c.348+5755del MANE Select	NP_057440.2:n.348+5755del
NM_001195610.2:c.348+5755del	NP_001182539.1:n.348+5755del