Canonical Allele Identifier: CA1910031172
Gene: DKK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52315282A= , CM000672.2:g.52315282A= GRCh38
NC_000010.10:g.54075042A= , CM000672.1:g.54075042A= GRCh37
NC_000010.9:g.53745048A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000373970.4:c.406+197A= MANE Select ENSP00000363081.3:n.406+197A=
ENST00000373970.3:c.406+197A= ENSP00000363081.3:n.406+197A=
ENST00000467359.5:n.406+197A=
ENST00000476752.1:n.31A=
ENST00000494277.5:n.29+197A=
NM_012242.2:c.406+197A= NP_036374.1:n.406+197A=
NM_012242.3:c.406+197A= NP_036374.1:n.406+197A=
NM_012242.4:c.406+197A= MANE Select NP_036374.1:n.406+197A=
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