Canonical Allele Identifier: CA566214940

Gene: DCDC2

Linked Data

• dbSNP Id: rs1433146749
• gnomAD v2: 6-24204881-GGTAA-G
• gnomAD v3: 6-24204653-GGTAA-G
• gnomAD v4: 6-24204653-GGTAA-G
• MyVariant Identifiers: chr6:g.24204882_24204885del (hg19) ; chr6:g.24204654_24204657del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24204657_24204660del , CM000668.2:g.24204657_24204660del	GRCh38
NC_000006.11:g.24204885_24204888del , CM000668.1:g.24204885_24204888del	GRCh37
NC_000006.10:g.24312864_24312867del	NCBI36
NG_012829.1:g.158396_158399del
NG_012829.2:g.183636_183639del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1023+345_1023+348del MANE Select	ENSP00000367715.3:n.1023+345_1023+348del
ENST00000378450.6:c.282+345_282+348del	ENSP00000367711.3:n.282+345_282+348del
ENST00000378454.7:c.1023+345_1023+348del	ENSP00000367715.3:n.1023+345_1023+348del
NM_001195610.1:c.1023+345_1023+348del	NP_001182539.1:n.1023+345_1023+348del
NM_016356.4:c.1023+345_1023+348del	NP_057440.2:n.1023+345_1023+348del
NM_016356.5:c.1023+345_1023+348del MANE Select	NP_057440.2:n.1023+345_1023+348del
NM_001195610.2:c.1023+345_1023+348del	NP_001182539.1:n.1023+345_1023+348del