Canonical Allele Identifier: CA1616386078
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206847T= , CM000668.2:g.24206847T= GRCh38
NC_000006.11:g.24207075T= , CM000668.1:g.24207075T= GRCh37
NC_000006.10:g.24315054T= NCBI36
NG_012829.1:g.156206A=
NG_012829.2:g.181446A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.923-1745A= MANE Select ENSP00000367715.3:n.923-1745A=
ENST00000378454.7:c.923-1745A= ENSP00000367715.3:n.923-1745A=
NM_001195610.1:c.923-1745A= NP_001182539.1:n.923-1745A=
NM_016356.4:c.923-1745A= NP_057440.2:n.923-1745A=
NM_016356.5:c.923-1745A= MANE Select NP_057440.2:n.923-1745A=
NM_001195610.2:c.923-1745A= NP_001182539.1:n.923-1745A=