Canonical Allele Identifier: CA1616325395
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178248_24178252delinsCTTGA , CM000668.2:g.24178248_24178252delinsCTTGA GRCh38
NC_000006.11:g.24178476_24178480delinsCTTGA , CM000668.1:g.24178476_24178480delinsCTTGA GRCh37
NC_000006.10:g.24286455_24286459delinsCTTGA NCBI36
NG_012829.1:g.184801_184805delinsTCAAG
NG_012829.2:g.210041_210045delinsTCAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+78_1326+82delinsTCAAG MANE Select ENSP00000367715.3:n.1326+78_1326+82delins...
ENST00000378450.6:c.585+78_585+82delinsTCAAG ENSP00000367711.3:n.585+78_585+82delinsTC...
ENST00000378454.7:c.1326+78_1326+82delinsTCAAG ENSP00000367715.3:n.1326+78_1326+82delins...
NM_001195610.1:c.1326+78_1326+82delinsTCAAG NP_001182539.1:n.1326+78_1326+82delinsTCA...
NM_016356.4:c.1326+78_1326+82delinsTCAAG NP_057440.2:n.1326+78_1326+82delinsTCAAG
NM_016356.5:c.1326+78_1326+82delinsTCAAG MANE Select NP_057440.2:n.1326+78_1326+82delinsTCAAG
NM_001195610.2:c.1326+78_1326+82delinsTCAAG NP_001182539.1:n.1326+78_1326+82delinsTCA...