Canonical Allele Identifier: CA13437463

Gene: DKK3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.11967604C>G , CM000673.2:g.11967604C>G	GRCh38
NC_000011.9:g.11989151C>G , CM000673.1:g.11989151C>G	GRCh37
NC_000011.8:g.11945727C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683431.1:c.529-506G>C MANE Select	ENSP00000506835.1:n.529-506G>C
ENST00000396505.7:c.529-506G>C	ENSP00000379762.2:n.529-506G>C
ENST00000326932.8:c.529-506G>C	ENSP00000314910.4:n.529-506G>C
ENST00000396505.6:c.529-506G>C	ENSP00000379762.2:n.529-506G>C
ENST00000525493.5:c.529-506G>C	ENSP00000433112.1:n.529-506G>C
ENST00000525927.5:n.325-506G>C
ENST00000527132.1:n.262-3135G>C
ENST00000528188.5:n.193-506G>C
ENST00000532372.5:n.353-506G>C
ENST00000532873.5:n.344-506G>C
ENST00000533813.5:c.529-506G>C	ENSP00000435269.1:n.529-506G>C
ENST00000534511.5:c.445-506G>C	ENSP00000436645.1:n.445-506G>C
NM_001018057.1:c.529-506G>C	NP_001018067.1:n.529-506G>C
NM_013253.4:c.529-506G>C	NP_037385.2:n.529-506G>C
NM_015881.5:c.529-506G>C	NP_056965.3:n.529-506G>C
XM_006718178.2:c.529-506G>C	XP_006718241.1:n.529-506G>C
NM_001330220.1:c.529-506G>C	NP_001317149.1:n.529-506G>C
XM_017017554.2:c.529-506G>C	XP_016873043.1:n.529-506G>C
XM_017017555.1:c.529-506G>C	XP_016873044.1:n.529-506G>C
NM_001330220.2:c.529-506G>C	NP_001317149.1:n.529-506G>C
NM_001018057.2:c.529-506G>C MANE Select	NP_001018067.1:n.529-506G>C
NM_001330220.3:c.529-506G>C	NP_001317149.1:n.529-506G>C
NM_013253.5:c.529-506G>C	NP_037385.2:n.529-506G>C
NM_015881.6:c.529-506G>C	NP_056965.3:n.529-506G>C