Canonical Allele Identifier: CA917697766

Gene: DCDC2

Linked Data

• dbSNP Id: rs1554144829

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24204846_24204847insC , CM000668.2:g.24204846_24204847insC	GRCh38
NC_000006.11:g.24205074_24205075insC , CM000668.1:g.24205074_24205075insC	GRCh37
NC_000006.10:g.24313053_24313054insC	NCBI36
NG_012829.1:g.158206_158207insG
NG_012829.2:g.183446_183447insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1023+155_1023+156insG MANE Select	ENSP00000367715.3:n.1023+155_1023+156insG
ENST00000378450.6:c.282+155_282+156insG	ENSP00000367711.3:n.282+155_282+156insG
ENST00000378454.7:c.1023+155_1023+156insG	ENSP00000367715.3:n.1023+155_1023+156insG
NM_001195610.1:c.1023+155_1023+156insG	NP_001182539.1:n.1023+155_1023+156insG
NM_016356.4:c.1023+155_1023+156insG	NP_057440.2:n.1023+155_1023+156insG
NM_016356.5:c.1023+155_1023+156insG MANE Select	NP_057440.2:n.1023+155_1023+156insG
NM_001195610.2:c.1023+155_1023+156insG	NP_001182539.1:n.1023+155_1023+156insG