Canonical Allele Identifier: CA566291226

Gene: DCDC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24178247A>T , CM000668.2:g.24178247A>T	GRCh38
NC_000006.11:g.24178475A>T , CM000668.1:g.24178475A>T	GRCh37
NC_000006.10:g.24286454A>T	NCBI36
NG_012829.1:g.184806T>A
NG_012829.2:g.210046T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1326+83T>A MANE Select	ENSP00000367715.3:n.1326+83T>A
ENST00000378450.6:c.585+83T>A	ENSP00000367711.3:n.585+83T>A
ENST00000378454.7:c.1326+83T>A	ENSP00000367715.3:n.1326+83T>A
NM_001195610.1:c.1326+83T>A	NP_001182539.1:n.1326+83T>A
NM_016356.4:c.1326+83T>A	NP_057440.2:n.1326+83T>A
NM_016356.5:c.1326+83T>A MANE Select	NP_057440.2:n.1326+83T>A
NM_001195610.2:c.1326+83T>A	NP_001182539.1:n.1326+83T>A