Canonical Allele Identifier: CA1616429000
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278696C= , CM000668.2:g.24278696C= GRCh38
NC_000006.11:g.24278924C= , CM000668.1:g.24278924C= GRCh37
NC_000006.10:g.24386903C= NCBI36
NG_012829.1:g.84357G=
NG_012829.2:g.109597G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.760-485G= MANE Select ENSP00000367715.3:n.760-485G=
ENST00000378454.7:c.760-485G= ENSP00000367715.3:n.760-485G=
NM_001195610.1:c.760-485G= NP_001182539.1:n.760-485G=
NM_016356.4:c.760-485G= NP_057440.2:n.760-485G=
NM_016356.5:c.760-485G= MANE Select NP_057440.2:n.760-485G=
NM_001195610.2:c.760-485G= NP_001182539.1:n.760-485G=