Canonical Allele Identifier: CA2677514351

Gene: DCDC2

Linked Data

• gnomAD v4: 6-24178296-C-CATT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24178297_24178299dup , CM000668.2:g.24178297_24178299dup	GRCh38
NC_000006.11:g.24178525_24178527dup , CM000668.1:g.24178525_24178527dup	GRCh37
NC_000006.10:g.24286504_24286506dup	NCBI36
NG_012829.1:g.184754_184756dup
NG_012829.2:g.209994_209996dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.1326+31_1326+33dup MANE Select	ENSP00000367715.3:n.1326+31_1326+33dup
ENST00000378450.6:c.585+31_585+33dup	ENSP00000367711.3:n.585+31_585+33dup
ENST00000378454.7:c.1326+31_1326+33dup	ENSP00000367715.3:n.1326+31_1326+33dup
NM_001195610.1:c.1326+31_1326+33dup	NP_001182539.1:n.1326+31_1326+33dup
NM_016356.4:c.1326+31_1326+33dup	NP_057440.2:n.1326+31_1326+33dup
NM_016356.5:c.1326+31_1326+33dup MANE Select	NP_057440.2:n.1326+31_1326+33dup
NM_001195610.2:c.1326+31_1326+33dup	NP_001182539.1:n.1326+31_1326+33dup