Canonical Allele Identifier: CA379466595

Gene: ILK TAF10

Linked Data

• gnomAD v4: 11-6610027-C-T
• MyVariant Identifiers: chr11:g.6631258C>T (hg19) ; chr11:g.6610027C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6610027C>T , CM000673.2:g.6610027C>T	GRCh38
NC_000011.9:g.6631258C>T , CM000673.1:g.6631258C>T	GRCh37
NC_000011.8:g.6587834C>T	NCBI36
NG_029702.1:g.11295C>T , LRG_444:g.11295C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299421.9:c.1070C>T (ILK) MANE Select	ENSP00000299421.4:p.Ala357Val
ENST00000299424.9:c.*895G>A (TAF10) MANE Select	ENSP00000299424.4:n.*895G>A
ENST00000299421.8:c.1070C>T (ILK)	ENSP00000299421.3:p.Ala357Val
ENST00000396751.6:c.1070C>T (ILK)	ENSP00000379975.2:p.Ala357Val
ENST00000420936.6:c.1070C>T (ILK)	ENSP00000403487.2:p.Ala357Val
ENST00000526318.2:c.328-576C>T (ILK)	ENSP00000480597.1:n.328-576C>T
ENST00000526711.5:c.*781C>T (ILK)	ENSP00000479932.1:n.*781C>T
ENST00000528784.5:n.943C>T (ILK)
ENST00000528995.5:c.887C>T (ILK)	ENSP00000435323.1:p.Ala296Val
ENST00000530016.5:n.1407C>T (ILK)
ENST00000532063.5:c.668C>T (ILK)	ENSP00000434492.2:p.Ala223Val
ENST00000537806.5:c.1163C>T (ILK)	ENSP00000439606.2:p.Ala388Val
ENST00000616342.1:n.1661G>A (TAF10)
NM_001014794.2:c.1070C>T (ILK)	NP_001014794.1:p.Ala357Val
NM_001014795.2:c.1070C>T (ILK)	NP_001014795.1:p.Ala357Val
NM_001278441.1:c.887C>T (ILK)	NP_001265370.1:p.Ala296Val
NM_001278442.1:c.668C>T (ILK)	NP_001265371.1:p.Ala223Val
NM_004517.3:c.1070C>T (ILK)	NP_004508.1:p.Ala357Val
XM_005252904.3:c.1070C>T (ILK)	XP_005252961.1:p.Ala357Val
XM_005252905.1:c.668C>T (ILK)	XP_005252962.1:p.Ala223Val
XM_011520065.1:c.1070C>T (ILK)	XP_011518367.1:p.Ala357Val
XM_005252904.5:c.1070C>T (ILK)	XP_005252961.1:p.Ala357Val
XM_005252905.3:c.668C>T (ILK)	XP_005252962.1:p.Ala223Val
XM_017017672.1:c.917C>T (ILK)	XP_016873161.1:p.Ala306Val
XM_024448494.1:c.1163C>T (ILK)	XP_024304262.1:p.Ala388Val
XM_024448495.1:c.1163C>T (ILK)	XP_024304263.1:p.Ala388Val
XM_024448496.1:c.1163C>T (ILK)	XP_024304264.1:p.Ala388Val
XM_024448497.1:c.1163C>T (ILK)	XP_024304265.1:p.Ala388Val
XM_024448498.1:c.917C>T (ILK)	XP_024304266.1:p.Ala306Val
XM_024448499.1:c.917C>T (ILK)	XP_024304267.1:p.Ala306Val
XM_024448500.1:c.761C>T (ILK)	XP_024304268.1:p.Ala254Val
NM_006284.4:c.*895G>A (TAF10) MANE Select	NP_006275.1:n.*895G>A
NM_001014794.3:c.1070C>T (ILK)	NP_001014794.1:p.Ala357Val
NM_001014795.3:c.1070C>T (ILK)	NP_001014795.1:p.Ala357Val
NM_001278441.2:c.887C>T (ILK)	NP_001265370.1:p.Ala296Val
NM_004517.4:c.1070C>T (ILK) MANE Select	NP_004508.1:p.Ala357Val
NM_001278442.2:c.668C>T (ILK)	NP_001265371.1:p.Ala223Val