Canonical Allele Identifier: CA2677515372

Gene: DCDC2

Linked Data

• gnomAD v4: 6-24302163-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24302163A>C , CM000668.2:g.24302163A>C	GRCh38
NC_000006.11:g.24302391A>C , CM000668.1:g.24302391A>C	GRCh37
NC_000006.10:g.24410370A>C	NCBI36
NG_012829.1:g.60890T>G
NG_012829.2:g.86130T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.349-119T>G MANE Select	ENSP00000367715.3:n.349-119T>G
ENST00000378454.7:c.349-119T>G	ENSP00000367715.3:n.349-119T>G
NM_001195610.1:c.349-119T>G	NP_001182539.1:n.349-119T>G
NM_016356.4:c.349-119T>G	NP_057440.2:n.349-119T>G
NM_016356.5:c.349-119T>G MANE Select	NP_057440.2:n.349-119T>G
NM_001195610.2:c.349-119T>G	NP_001182539.1:n.349-119T>G