Canonical Allele Identifier: CA1616321971
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174744C= , CM000668.2:g.24174744C= GRCh38
NC_000006.11:g.24174972C= , CM000668.1:g.24174972C= GRCh37
NC_000006.10:g.24282951C= NCBI36
NG_012829.1:g.188309G=
NG_012829.2:g.213549G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1417G= MANE Select ENSP00000367715.3:p.Ala473=
ENST00000378450.6:c.676G= ENSP00000367711.3:p.Ala226=
ENST00000378454.7:c.1417G= ENSP00000367715.3:p.Ala473=
NM_001195610.1:c.1417G= NP_001182539.1:p.Ala473=
NM_016356.4:c.1417G= NP_057440.2:p.Ala473=
NM_016356.5:c.1417G= MANE Select NP_057440.2:p.Ala473=
NM_001195610.2:c.1417G= NP_001182539.1:p.Ala473=