Canonical Allele Identifier: CA1616325104
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178072_24178087delinsAGGTAAGTAGATGGAT , CM000668.2:g.24178072_24178087delinsAGGTAAGTAGATGGAT GRCh38
NC_000006.11:g.24178300_24178315delinsAGGTAAGTAGATGGAT , CM000668.1:g.24178300_24178315delinsAGGTAAGTAGATGGAT GRCh37
NC_000006.10:g.24286279_24286294delinsAGGTAAGTAGATGGAT NCBI36
NG_012829.1:g.184966_184981delinsATCCATCTACTTACCT
NG_012829.2:g.210206_210221delinsATCCATCTACTTACCT

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+243_1326+258delinsATCCATCTACTTACCT MANE Select ENSP00000367715.3:n.1326+243_1326+258deli...
ENST00000378450.6:c.585+243_585+258delinsATCCATCTACTTACCT ENSP00000367711.3:n.585+243_585+258delins...
ENST00000378454.7:c.1326+243_1326+258delinsATCCATCTACTTACCT ENSP00000367715.3:n.1326+243_1326+258deli...
NM_001195610.1:c.1326+243_1326+258delinsATCCATCTACTTACCT NP_001182539.1:n.1326+243_1326+258delinsA...
NM_016356.4:c.1326+243_1326+258delinsATCCATCTACTTACCT NP_057440.2:n.1326+243_1326+258delinsATCC...
NM_016356.5:c.1326+243_1326+258delinsATCCATCTACTTACCT MANE Select NP_057440.2:n.1326+243_1326+258delinsATCC...
NM_001195610.2:c.1326+243_1326+258delinsATCCATCTACTTACCT NP_001182539.1:n.1326+243_1326+258delinsA...