Canonical Allele Identifier: CA1616386009
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206709_24206712delinsAAAG , CM000668.2:g.24206709_24206712delinsAAAG GRCh38
NC_000006.11:g.24206937_24206940delinsAAAG , CM000668.1:g.24206937_24206940delinsAAAG GRCh37
NC_000006.10:g.24314916_24314919delinsAAAG NCBI36
NG_012829.1:g.156341_156344delinsCTTT
NG_012829.2:g.181581_181584delinsCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.923-1610_923-1607delinsCTTT MANE Select ENSP00000367715.3:n.923-1610_923-1607delinsCTTT
ENST00000378454.7:c.923-1610_923-1607delinsCTTT ENSP00000367715.3:n.923-1610_923-1607delinsCTTT
NM_001195610.1:c.923-1610_923-1607delinsCTTT NP_001182539.1:n.923-1610_923-1607delinsCTTT
NM_016356.4:c.923-1610_923-1607delinsCTTT NP_057440.2:n.923-1610_923-1607delinsCTTT
NM_016356.5:c.923-1610_923-1607delinsCTTT MANE Select NP_057440.2:n.923-1610_923-1607delinsCTTT
NM_001195610.2:c.923-1610_923-1607delinsCTTT NP_001182539.1:n.923-1610_923-1607delinsCTTT