Canonical Allele Identifier: CA5888828
Gene: DKK3 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.11968352T>C
GRCh37 chr11:g.11989899T>C
gnomAD v2:
11:11989899 T / C
gnomAD v3:
11:11968352 T / C
gnomAD v4:
chr11-11968352-T-C
Joint Max Group AF 0.94105002 (MID)
Genomes Max Group AF 0.92474646 (AFR)
Exomes Max Group AF 0.93959058 (MID)
dbSNP:
2291599
JSON-LD

Genomic Alleles

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

Transcript Alleles

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