Canonical Allele Identifier: CA566220799

Gene: DCDC2

Linked Data

• dbSNP Id: rs1449930134
• gnomAD v2: 6-24178271-CTG-C
• gnomAD v3: 6-24178043-CTG-C
• gnomAD v4: 6-24178043-CTG-C
• MyVariant Identifiers: chr6:g.24178272_24178273del (hg19) ; chr6:g.24178044_24178045del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24178045_24178046del , CM000668.2:g.24178045_24178046del	GRCh38
NC_000006.11:g.24178273_24178274del , CM000668.1:g.24178273_24178274del	GRCh37
NC_000006.10:g.24286252_24286253del	NCBI36
NG_012829.1:g.185008_185009del
NG_012829.2:g.210248_210249del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.1326+285_1326+286del MANE Select	ENSP00000367715.3:n.1326+285_1326+286del
ENST00000378450.6:c.585+285_585+286del	ENSP00000367711.3:n.585+285_585+286del
ENST00000378454.7:c.1326+285_1326+286del	ENSP00000367715.3:n.1326+285_1326+286del
NM_001195610.1:c.1326+285_1326+286del	NP_001182539.1:n.1326+285_1326+286del
NM_016356.4:c.1326+285_1326+286del	NP_057440.2:n.1326+285_1326+286del
NM_016356.5:c.1326+285_1326+286del MANE Select	NP_057440.2:n.1326+285_1326+286del
NM_001195610.2:c.1326+285_1326+286del	NP_001182539.1:n.1326+285_1326+286del