Canonical Allele Identifier: CA379457733

Gene: ILK TAF10

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6608694G>A , CM000673.2:g.6608694G>A	GRCh38
NC_000011.9:g.6629924G>A , CM000673.1:g.6629924G>A	GRCh37
NC_000011.8:g.6586500G>A	NCBI36
NG_029702.1:g.9961G>A , LRG_444:g.9961G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004517.4:c.352G>A (ILK) MANE Select	NP_004508.1:p.Asp118Asn
NM_006284.4:c.*2228C>T (TAF10) MANE Select	NP_006275.1:n.*2228C>T
ENST00000299421.9:c.352G>A (ILK) MANE Select	ENSP00000299421.4:p.Asp118Asn
ENST00000299424.9:c.*2228C>T (TAF10) MANE Select	ENSP00000299424.4:n.*2228C>T
NM_001014794.2:c.352G>A (ILK)	NP_001014794.1:p.Asp118Asn
NM_001014794.3:c.352G>A (ILK)	NP_001014794.1:p.Asp118Asn
NM_001014795.2:c.352G>A (ILK)	NP_001014795.1:p.Asp118Asn
NM_001014795.3:c.352G>A (ILK)	NP_001014795.1:p.Asp118Asn
NM_001278441.1:c.352-190G>A (ILK)	NP_001265370.1:n.352-190G>A
NM_001278441.2:c.352-190G>A (ILK)	NP_001265370.1:n.352-190G>A
NM_001278442.1:c.-51G>A (ILK)	NP_001265371.1:n.-51G>A
NM_001278442.2:c.-51G>A (ILK)	NP_001265371.1:n.-51G>A
NM_004517.3:c.352G>A (ILK)	NP_004508.1:p.Asp118Asn
ENST00000299421.8:c.352G>A (ILK)	ENSP00000299421.3:p.Asp118Asn
ENST00000396751.6:c.352G>A (ILK)	ENSP00000379975.2:p.Asp118Asn
ENST00000420936.6:c.352G>A (ILK)	ENSP00000403487.2:p.Asp118Asn
ENST00000526114.5:c.*332G>A (ILK)	ENSP00000432617.1:n.*332G>A
ENST00000526318.2:c.327+205G>A (ILK)	ENSP00000480597.1:n.327+205G>A
ENST00000526711.5:c.*63G>A (ILK)	ENSP00000479932.1:n.*63G>A
ENST00000527121.5:c.*332G>A (ILK)	ENSP00000436062.1:n.*332G>A
ENST00000528784.5:n.225G>A (ILK)
ENST00000528995.5:c.352-190G>A (ILK)	ENSP00000435323.1:n.352-190G>A
ENST00000530016.5:n.493G>A (ILK)
ENST00000532063.5:c.-51G>A (ILK)	ENSP00000434492.2:n.-51G>A
ENST00000537806.5:c.352G>A (ILK)	ENSP00000439606.2:p.Asp118Asn
ENST00000616342.1:n.2994C>T (TAF10)
XM_005252904.3:c.352G>A (ILK)	XP_005252961.1:p.Asp118Asn
XM_005252904.5:c.352G>A (ILK)	XP_005252961.1:p.Asp118Asn
XM_005252905.1:c.-51G>A (ILK)	XP_005252962.1:n.-51G>A
XM_005252905.3:c.-51G>A (ILK)	XP_005252962.1:n.-51G>A
XM_011520065.1:c.352G>A (ILK)	XP_011518367.1:p.Asp118Asn
XM_017017672.1:c.199G>A (ILK)	XP_016873161.1:p.Asp67Asn
XM_024448494.1:c.352G>A (ILK)	XP_024304262.1:p.Asp118Asn
XM_024448495.1:c.352G>A (ILK)	XP_024304263.1:p.Asp118Asn
XM_024448496.1:c.352G>A (ILK)	XP_024304264.1:p.Asp118Asn
XM_024448497.1:c.352G>A (ILK)	XP_024304265.1:p.Asp118Asn
XM_024448498.1:c.199G>A (ILK)	XP_024304266.1:p.Asp67Asn
XM_024448499.1:c.199G>A (ILK)	XP_024304267.1:p.Asp67Asn
XM_024448500.1:c.-51G>A (ILK)	XP_024304268.1:n.-51G>A
XR_001748110.1:n.28C>T