Canonical Allele Identifier: CA1483460622
Gene: DKK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.106932829T= , CM000666.2:g.106932829T= GRCh38
NC_000004.11:g.107853986T= , CM000666.1:g.107853986T= GRCh37
NC_000004.10:g.108073435T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000285311.8:c.223-6880A= MANE Select ENSP00000285311.3:n.223-6880A=
ENST00000285311.7:c.223-6880A= ENSP00000285311.3:n.223-6880A=
ENST00000510463.1:c.85-6880A= ENSP00000423797.1:n.85-6880A=
ENST00000510534.1:n.444-6880A=
ENST00000513208.5:c.-78-6880A= ENSP00000421255.1:n.-78-6880A=
NM_014421.2:c.223-6880A= NP_055236.1:n.223-6880A=
NM_014421.3:c.223-6880A= MANE Select NP_055236.1:n.223-6880A=