Canonical Allele Identifier: CA1616446799
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290974C= , CM000668.2:g.24290974C= GRCh38
NC_000006.11:g.24291202C= , CM000668.1:g.24291202C= GRCh37
NC_000006.10:g.24399181C= NCBI36
NG_012829.1:g.72079G=
NG_012829.2:g.97319G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.662G= MANE Select ENSP00000367715.3:p.Ser221=
ENST00000378454.7:c.662G= ENSP00000367715.3:p.Ser221=
NM_001195610.1:c.662G= NP_001182539.1:p.Ser221=
NM_016356.4:c.662G= NP_057440.2:p.Ser221=
NM_016356.5:c.662G= MANE Select NP_057440.2:p.Ser221=
NM_001195610.2:c.662G= NP_001182539.1:p.Ser221=