Canonical Allele Identifier: CA1616420489
Gene: DCDC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24273503T= , CM000668.2:g.24273503T= GRCh38
NC_000006.11:g.24273731T= , CM000668.1:g.24273731T= GRCh37
NC_000006.10:g.24381710T= NCBI36
NG_012829.1:g.89550A=
NG_012829.2:g.114790A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.922+4546A= MANE Select ENSP00000367715.3:n.922+4546A=
ENST00000378454.7:c.922+4546A= ENSP00000367715.3:n.922+4546A=
NM_001195610.1:c.922+4546A= NP_001182539.1:n.922+4546A=
NM_016356.4:c.922+4546A= NP_057440.2:n.922+4546A=
NM_016356.5:c.922+4546A= MANE Select NP_057440.2:n.922+4546A=
NM_001195610.2:c.922+4546A= NP_001182539.1:n.922+4546A=
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