Canonical Allele Identifier: CA378317126

Gene: WDR11

Linked Data

• MyVariant Identifiers: chr10:g.122666298T>C (hg19) ; chr10:g.120906786T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.120906786T>C , CM000672.2:g.120906786T>C	GRCh38
NC_000010.10:g.122666298T>C , CM000672.1:g.122666298T>C	GRCh37
NC_000010.9:g.122656288T>C	NCBI36
NG_023290.1:g.60612T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263461.11:c.3448T>C MANE Select	ENSP00000263461.5:p.Phe1150Leu
ENST00000263461.10:c.3448T>C	ENSP00000263461.5:p.Phe1150Leu
ENST00000497136.6:c.*2721T>C	ENSP00000474595.1:n.*2721T>C
ENST00000604509.5:n.3877T>C
ENST00000605543.5:c.*1967T>C	ENSP00000475076.1:n.*1967T>C
NM_018117.11:c.3448T>C	NP_060587.8:p.Phe1150Leu
XM_005269962.1:c.2671T>C	XP_005270019.1:p.Phe891Leu
XM_005269963.1:c.2671T>C	XP_005270020.1:p.Phe891Leu
XM_005269964.1:c.2035T>C	XP_005270021.1:p.Phe679Leu
XR_428707.1:n.3439T>C
XR_946372.1:n.253-4444A>G
XM_005269963.2:c.2671T>C	XP_005270020.1:p.Phe891Leu
XM_017016397.1:c.3274T>C	XP_016871886.1:p.Phe1092Leu
XM_017016398.1:c.2671T>C	XP_016871887.1:p.Phe891Leu
XM_017016399.1:c.2161T>C	XP_016871888.1:p.Phe721Leu
XM_024448075.1:c.2035T>C	XP_024303843.1:p.Phe679Leu
XR_001747136.2:n.3357T>C
XR_001747137.2:n.3211T>C
XR_001747609.1:n.541-4444A>G
XR_428707.3:n.3383T>C
XR_946372.2:n.1156-4444A>G
NM_018117.12:c.3448T>C MANE Select	NP_060587.8:p.Phe1150Leu