Canonical Allele Identifier: CA12037345
Gene: CDC25C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138306341C>T , CM000667.2:g.138306341C>T GRCh38
NC_000005.9:g.137642030C>T , CM000667.1:g.137642030C>T GRCh37
NC_000005.8:g.137669929C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000323760.11:c.615+12878G>A MANE Select ENSP00000321656.6:n.615+12878G>A
ENST00000648466.1:c.*72-2659G>A ENSP00000497591.1:n.*72-2659G>A
ENST00000323760.10:c.615+12878G>A ENSP00000321656.6:n.615+12878G>A
ENST00000348983.7:c.396+12878G>A ENSP00000345205.3:n.396+12878G>A
ENST00000415130.6:c.396+12878G>A ENSP00000392631.2:n.396+12878G>A
ENST00000503022.5:c.615+12878G>A ENSP00000427251.1:n.615+12878G>A
ENST00000513970.5:c.615+12878G>A ENSP00000424795.1:n.615+12878G>A
ENST00000514555.5:c.525+12878G>A ENSP00000425470.1:n.525+12878G>A
NM_001287582.1:c.615+12878G>A NP_001274511.1:n.615+12878G>A
NM_001287583.1:c.849+12878G>A NP_001274512.1:n.849+12878G>A
NM_001790.4:c.615+12878G>A NP_001781.2:n.615+12878G>A
NM_022809.3:c.396+12878G>A NP_073720.1:n.396+12878G>A
XM_005272145.2:c.849+12878G>A XP_005272202.1:n.849+12878G>A
XM_005272146.3:c.666+12878G>A XP_005272203.1:n.666+12878G>A
XM_006714739.2:c.621+12878G>A XP_006714802.1:n.621+12878G>A
XM_011543759.1:c.687+12878G>A XP_011542061.1:n.687+12878G>A
XM_011543760.1:c.849+12878G>A XP_011542062.1:n.849+12878G>A
XM_011543761.1:c.630+12878G>A XP_011542063.1:n.630+12878G>A
XM_011543762.1:c.396+12878G>A XP_011542064.1:n.396+12878G>A
XM_011543763.1:c.282+12878G>A XP_011542065.1:n.282+12878G>A
XM_011543764.1:c.129+12878G>A XP_011542066.1:n.129+12878G>A
NM_001318098.1:c.666+12878G>A NP_001305027.1:n.666+12878G>A
NM_001364026.1:c.849+12878G>A NP_001350955.1:n.849+12878G>A
NM_001364027.1:c.615+12878G>A NP_001350956.1:n.615+12878G>A
NM_001364028.1:c.486+12878G>A NP_001350957.1:n.486+12878G>A
XM_005272145.3:c.849+12878G>A XP_005272202.1:n.849+12878G>A
XM_006714739.3:c.621+12878G>A XP_006714802.1:n.621+12878G>A
XM_011543759.3:c.687+12878G>A XP_011542061.1:n.687+12878G>A
XM_011543760.2:c.849+12878G>A XP_011542062.1:n.849+12878G>A
XM_011543761.2:c.630+12878G>A XP_011542063.1:n.630+12878G>A
NM_001790.5:c.615+12878G>A MANE Select NP_001781.2:n.615+12878G>A
NM_001287582.2:c.615+12878G>A NP_001274511.1:n.615+12878G>A
NM_001287583.2:c.849+12878G>A NP_001274512.1:n.849+12878G>A
NM_001318098.2:c.666+12878G>A NP_001305027.1:n.666+12878G>A
NM_022809.4:c.396+12878G>A NP_073720.1:n.396+12878G>A
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