Canonical Allele Identifier: CA823270681

Gene: DCDC2

Linked Data

• dbSNP Id: rs1177195675
• gnomAD v3: 6-24204856-TTA-T
• gnomAD v4: 6-24204856-TTA-T
• MyVariant Identifiers: chr6:g.24205085_24205086del (hg19) ; chr6:g.24204857_24204858del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24204858_24204859del , CM000668.2:g.24204858_24204859del	GRCh38
NC_000006.11:g.24205086_24205087del , CM000668.1:g.24205086_24205087del	GRCh37
NC_000006.10:g.24313065_24313066del	NCBI36
NG_012829.1:g.158195_158196del
NG_012829.2:g.183435_183436del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1023+144_1023+145del MANE Select	ENSP00000367715.3:n.1023+144_1023+145del
ENST00000378450.6:c.282+144_282+145del	ENSP00000367711.3:n.282+144_282+145del
ENST00000378454.7:c.1023+144_1023+145del	ENSP00000367715.3:n.1023+144_1023+145del
NM_001195610.1:c.1023+144_1023+145del	NP_001182539.1:n.1023+144_1023+145del
NM_016356.4:c.1023+144_1023+145del	NP_057440.2:n.1023+144_1023+145del
NM_016356.5:c.1023+144_1023+145del MANE Select	NP_057440.2:n.1023+144_1023+145del
NM_001195610.2:c.1023+144_1023+145del	NP_001182539.1:n.1023+144_1023+145del