Canonical Allele Identifier: CA566215097

Gene: DCDC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24206652dup , CM000668.2:g.24206652dup	GRCh38
NC_000006.11:g.24206880dup , CM000668.1:g.24206880dup	GRCh37
NC_000006.10:g.24314859dup	NCBI36
NG_012829.1:g.156401dup
NG_012829.2:g.181641dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.923-1550dup MANE Select	ENSP00000367715.3:n.923-1550dup
ENST00000378454.7:c.923-1550dup	ENSP00000367715.3:n.923-1550dup
NM_001195610.1:c.923-1550dup	NP_001182539.1:n.923-1550dup
NM_016356.4:c.923-1550dup	NP_057440.2:n.923-1550dup
NM_016356.5:c.923-1550dup MANE Select	NP_057440.2:n.923-1550dup
NM_001195610.2:c.923-1550dup	NP_001182539.1:n.923-1550dup