Canonical Allele Identifier: CA1086942334

Gene: DCDC2

Linked Data

• dbSNP Id: rs1759391227
• gnomAD v3: 6-24302161-A-AAAG
• gnomAD v4: 6-24302161-A-AAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24302163_24302164insGAA , CM000668.2:g.24302163_24302164insGAA	GRCh38
NC_000006.11:g.24302391_24302392insGAA , CM000668.1:g.24302391_24302392insGAA	GRCh37
NC_000006.10:g.24410370_24410371insGAA	NCBI36
NG_012829.1:g.60891_60892insCTT
NG_012829.2:g.86131_86132insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.349-118_349-117insCTT MANE Select	ENSP00000367715.3:n.349-118_349-117insCTT
ENST00000378454.7:c.349-118_349-117insCTT	ENSP00000367715.3:n.349-118_349-117insCTT
NM_001195610.1:c.349-118_349-117insCTT	NP_001182539.1:n.349-118_349-117insCTT
NM_016356.4:c.349-118_349-117insCTT	NP_057440.2:n.349-118_349-117insCTT
NM_016356.5:c.349-118_349-117insCTT MANE Select	NP_057440.2:n.349-118_349-117insCTT
NM_001195610.2:c.349-118_349-117insCTT	NP_001182539.1:n.349-118_349-117insCTT