Canonical Allele Identifier: CA1616417078
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306277_24306279delinsCTT , CM000668.2:g.24306277_24306279delinsCTT GRCh38
NC_000006.11:g.24306505_24306507delinsCTT , CM000668.1:g.24306505_24306507delinsCTT GRCh37
NC_000006.10:g.24414484_24414486delinsCTT NCBI36
NG_012829.1:g.56774_56776delinsAAG
NG_012829.2:g.82014_82016delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.349-4235_349-4233delinsAAG MANE Select ENSP00000367715.3:n.349-4235_349-4233delinsAAG
ENST00000378454.7:c.349-4235_349-4233delinsAAG ENSP00000367715.3:n.349-4235_349-4233delinsAAG
NM_001195610.1:c.349-4235_349-4233delinsAAG NP_001182539.1:n.349-4235_349-4233delinsAAG
NM_016356.4:c.349-4235_349-4233delinsAAG NP_057440.2:n.349-4235_349-4233delinsAAG
NM_016356.5:c.349-4235_349-4233delinsAAG MANE Select NP_057440.2:n.349-4235_349-4233delinsAAG
NM_001195610.2:c.349-4235_349-4233delinsAAG NP_001182539.1:n.349-4235_349-4233delinsAAG