Canonical Allele Identifier: CA823286367

Gene: DCDC2

Linked Data

• dbSNP Id: rs1274718805
• gnomAD v3: 6-24177993-TCTTA-T
• gnomAD v4: 6-24177993-TCTTA-T
• MyVariant Identifiers: chr6:g.24178222_24178225del (hg19) ; chr6:g.24177994_24177997del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24177997_24178000del , CM000668.2:g.24177997_24178000del	GRCh38
NC_000006.11:g.24178225_24178228del , CM000668.1:g.24178225_24178228del	GRCh37
NC_000006.10:g.24286204_24286207del	NCBI36
NG_012829.1:g.185056_185059del
NG_012829.2:g.210296_210299del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.1326+333_1326+336del MANE Select	ENSP00000367715.3:n.1326+333_1326+336del
ENST00000378450.6:c.585+333_585+336del	ENSP00000367711.3:n.585+333_585+336del
ENST00000378454.7:c.1326+333_1326+336del	ENSP00000367715.3:n.1326+333_1326+336del
NM_001195610.1:c.1326+333_1326+336del	NP_001182539.1:n.1326+333_1326+336del
NM_016356.4:c.1326+333_1326+336del	NP_057440.2:n.1326+333_1326+336del
NM_016356.5:c.1326+333_1326+336del MANE Select	NP_057440.2:n.1326+333_1326+336del
NM_001195610.2:c.1326+333_1326+336del	NP_001182539.1:n.1326+333_1326+336del