Canonical Allele Identifier: CA566215100

Gene: DCDC2

Linked Data

• dbSNP Id: rs1447250635
• gnomAD v2: 6-24206937-AAAG-A
• gnomAD v3: 6-24206709-AAAG-A
• gnomAD v4: 6-24206709-AAAG-A
• MyVariant Identifiers: chr6:g.24206938_24206940del (hg19) ; chr6:g.24206710_24206712del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24206715_24206717del , CM000668.2:g.24206715_24206717del	GRCh38
NC_000006.11:g.24206943_24206945del , CM000668.1:g.24206943_24206945del	GRCh37
NC_000006.10:g.24314922_24314924del	NCBI36
NG_012829.1:g.156341_156343del
NG_012829.2:g.181581_181583del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.923-1610_923-1608del MANE Select	ENSP00000367715.3:n.923-1610_923-1608del
ENST00000378454.7:c.923-1610_923-1608del	ENSP00000367715.3:n.923-1610_923-1608del
NM_001195610.1:c.923-1610_923-1608del	NP_001182539.1:n.923-1610_923-1608del
NM_016356.4:c.923-1610_923-1608del	NP_057440.2:n.923-1610_923-1608del
NM_016356.5:c.923-1610_923-1608del MANE Select	NP_057440.2:n.923-1610_923-1608del
NM_001195610.2:c.923-1610_923-1608del	NP_001182539.1:n.923-1610_923-1608del