Canonical Allele Identifier: CA1616385103
Gene: DCDC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24204625T= , CM000668.2:g.24204625T= GRCh38
NC_000006.11:g.24204853T= , CM000668.1:g.24204853T= GRCh37
NC_000006.10:g.24312832T= NCBI36
NG_012829.1:g.158428A=
NG_012829.2:g.183668A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1023+377A= MANE Select ENSP00000367715.3:n.1023+377A=
ENST00000378450.6:c.282+377A= ENSP00000367711.3:n.282+377A=
ENST00000378454.7:c.1023+377A= ENSP00000367715.3:n.1023+377A=
NM_001195610.1:c.1023+377A= NP_001182539.1:n.1023+377A=
NM_016356.4:c.1023+377A= NP_057440.2:n.1023+377A=
NM_016356.5:c.1023+377A= MANE Select NP_057440.2:n.1023+377A=
NM_001195610.2:c.1023+377A= NP_001182539.1:n.1023+377A=
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