Canonical Allele Identifier: CA136625652

Gene: DCDC2

Linked Data

• dbSNP Id: rs954366874
• gnomAD v2: 6-24204946-CTT-C
• gnomAD v3: 6-24204718-CTT-C
• gnomAD v4: 6-24204718-CTT-C
• MyVariant Identifiers: chr6:g.24204947_24204948del (hg19) ; chr6:g.24204719_24204720del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24204720_24204721del , CM000668.2:g.24204720_24204721del	GRCh38
NC_000006.11:g.24204948_24204949del , CM000668.1:g.24204948_24204949del	GRCh37
NC_000006.10:g.24312927_24312928del	NCBI36
NG_012829.1:g.158333_158334del
NG_012829.2:g.183573_183574del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1023+282_1023+283del MANE Select	ENSP00000367715.3:n.1023+282_1023+283del
ENST00000378450.6:c.282+282_282+283del	ENSP00000367711.3:n.282+282_282+283del
ENST00000378454.7:c.1023+282_1023+283del	ENSP00000367715.3:n.1023+282_1023+283del
NM_001195610.1:c.1023+282_1023+283del	NP_001182539.1:n.1023+282_1023+283del
NM_016356.4:c.1023+282_1023+283del	NP_057440.2:n.1023+282_1023+283del
NM_016356.5:c.1023+282_1023+283del MANE Select	NP_057440.2:n.1023+282_1023+283del
NM_001195610.2:c.1023+282_1023+283del	NP_001182539.1:n.1023+282_1023+283del