Canonical Allele Identifier: CA14624123
Gene: WDR7 HGNC NCBI

Linked Data

dbSNP Id: rs17750015

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.56730391T>C , CM000680.2:g.56730391T>C GRCh38
NC_000018.9:g.54397622T>C , CM000680.1:g.54397622T>C GRCh37
NC_000018.8:g.52548620T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000254442.8:c.1775-992T>C MANE Select ENSP00000254442.3:n.1775-992T>C
ENST00000254442.7:c.1775-992T>C ENSP00000254442.3:n.1775-992T>C
ENST00000357574.7:c.1775-992T>C ENSP00000350187.2:n.1775-992T>C
ENST00000585824.1:n.173-992T>C
ENST00000587403.5:n.221-992T>C
ENST00000589935.1:c.-1+78815T>C ENSP00000467485.1:n.-1+78815T>C
ENST00000590557.5:n.100-992T>C
ENST00000615645.4:c.194-26421T>C ENSP00000481823.1:n.194-26421T>C
NM_015285.2:c.1775-992T>C NP_056100.2:n.1775-992T>C
NM_052834.2:c.1775-992T>C NP_443066.2:n.1775-992T>C
XM_005266674.2:c.251-992T>C XP_005266731.1:n.251-992T>C
XM_006722431.1:c.1775-992T>C XP_006722494.1:n.1775-992T>C
XM_011525888.1:c.1775-992T>C XP_011524190.1:n.1775-992T>C
XM_006722431.2:c.1775-992T>C XP_006722494.1:n.1775-992T>C
XM_011525888.2:c.1775-992T>C XP_011524190.1:n.1775-992T>C
XM_017025682.1:c.1775-992T>C XP_016881171.1:n.1775-992T>C
XM_017025683.1:c.251-992T>C XP_016881172.1:n.251-992T>C
XR_001753170.2:n.2012-992T>C
XR_001753171.2:n.2012-992T>C
NM_001382485.1:c.1775-992T>C NP_001369414.1:n.1775-992T>C
NM_001382487.1:c.1775-992T>C NP_001369416.1:n.1775-992T>C
NM_015285.3:c.1775-992T>C MANE Select NP_056100.2:n.1775-992T>C
NM_052834.3:c.1775-992T>C NP_443066.2:n.1775-992T>C