Canonical Allele Identifier: CA1952604379
Gene: DKK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.11968352T>A , CM000673.2:g.11968352T>A GRCh38
NC_000011.9:g.11989899T>A , CM000673.1:g.11989899T>A GRCh37
NC_000011.8:g.11946475T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000683431.1:c.528+43A>T MANE Select ENSP00000506835.1:n.528+43A>T
ENST00000396505.7:c.528+43A>T ENSP00000379762.2:n.528+43A>T
ENST00000326932.8:c.528+43A>T ENSP00000314910.4:n.528+43A>T
ENST00000396505.6:c.528+43A>T ENSP00000379762.2:n.528+43A>T
ENST00000525493.5:c.528+43A>T ENSP00000433112.1:n.528+43A>T
ENST00000525927.5:n.324+43A>T
ENST00000527132.1:n.262-3883A>T
ENST00000528188.5:n.192+43A>T
ENST00000532372.5:n.352+43A>T
ENST00000532873.5:n.343+43A>T
ENST00000533813.5:c.528+43A>T ENSP00000435269.1:n.528+43A>T
ENST00000534511.5:c.444+43A>T ENSP00000436645.1:n.444+43A>T
NM_001018057.1:c.528+43A>T NP_001018067.1:n.528+43A>T
NM_013253.4:c.528+43A>T NP_037385.2:n.528+43A>T
NM_015881.5:c.528+43A>T NP_056965.3:n.528+43A>T
XM_006718178.2:c.528+43A>T XP_006718241.1:n.528+43A>T
NM_001330220.1:c.528+43A>T NP_001317149.1:n.528+43A>T
XM_017017554.2:c.528+43A>T XP_016873043.1:n.528+43A>T
XM_017017555.1:c.528+43A>T XP_016873044.1:n.528+43A>T
NM_001330220.2:c.528+43A>T NP_001317149.1:n.528+43A>T
NM_001018057.2:c.528+43A>T MANE Select NP_001018067.1:n.528+43A>T
NM_001330220.3:c.528+43A>T NP_001317149.1:n.528+43A>T
NM_013253.5:c.528+43A>T NP_037385.2:n.528+43A>T
NM_015881.6:c.528+43A>T NP_056965.3:n.528+43A>T