Canonical Allele Identifier: CA2612255397

Gene: ILK TAF10

Linked Data

• gnomAD v4: 11-6609888-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6609888T>A , CM000673.2:g.6609888T>A	GRCh38
NC_000011.9:g.6631119T>A , CM000673.1:g.6631119T>A	GRCh37
NC_000011.8:g.6587695T>A	NCBI36
NG_029702.1:g.11156T>A , LRG_444:g.11156T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299421.9:c.978+43T>A (ILK) MANE Select	ENSP00000299421.4:n.978+43T>A
ENST00000299424.9:c.*1034A>T (TAF10) MANE Select	ENSP00000299424.4:n.*1034A>T
ENST00000299421.8:c.978+43T>A (ILK)	ENSP00000299421.3:n.978+43T>A
ENST00000396751.6:c.978+43T>A (ILK)	ENSP00000379975.2:n.978+43T>A
ENST00000420936.6:c.978+43T>A (ILK)	ENSP00000403487.2:n.978+43T>A
ENST00000526318.2:c.328-715T>A (ILK)	ENSP00000480597.1:n.328-715T>A
ENST00000526711.5:c.*689+43T>A (ILK)	ENSP00000479932.1:n.*689+43T>A
ENST00000528784.5:n.851+43T>A (ILK)
ENST00000528995.5:c.795+43T>A (ILK)	ENSP00000435323.1:n.795+43T>A
ENST00000530016.5:n.1315+43T>A (ILK)
ENST00000532063.5:c.576+43T>A (ILK)	ENSP00000434492.2:n.576+43T>A
ENST00000537806.5:c.1071+43T>A (ILK)	ENSP00000439606.2:n.1071+43T>A
ENST00000616342.1:n.1800A>T (TAF10)
NM_001014794.2:c.978+43T>A (ILK)	NP_001014794.1:n.978+43T>A
NM_001014795.2:c.978+43T>A (ILK)	NP_001014795.1:n.978+43T>A
NM_001278441.1:c.795+43T>A (ILK)	NP_001265370.1:n.795+43T>A
NM_001278442.1:c.576+43T>A (ILK)	NP_001265371.1:n.576+43T>A
NM_004517.3:c.978+43T>A (ILK)	NP_004508.1:n.978+43T>A
XM_005252904.3:c.978+43T>A (ILK)	XP_005252961.1:n.978+43T>A
XM_005252905.1:c.576+43T>A (ILK)	XP_005252962.1:n.576+43T>A
XM_011520065.1:c.978+43T>A (ILK)	XP_011518367.1:n.978+43T>A
XM_005252904.5:c.978+43T>A (ILK)	XP_005252961.1:n.978+43T>A
XM_005252905.3:c.576+43T>A (ILK)	XP_005252962.1:n.576+43T>A
XM_017017672.1:c.825+43T>A (ILK)	XP_016873161.1:n.825+43T>A
XM_024448494.1:c.1071+43T>A (ILK)	XP_024304262.1:n.1071+43T>A
XM_024448495.1:c.1071+43T>A (ILK)	XP_024304263.1:n.1071+43T>A
XM_024448496.1:c.1071+43T>A (ILK)	XP_024304264.1:n.1071+43T>A
XM_024448497.1:c.1071+43T>A (ILK)	XP_024304265.1:n.1071+43T>A
XM_024448498.1:c.825+43T>A (ILK)	XP_024304266.1:n.825+43T>A
XM_024448499.1:c.825+43T>A (ILK)	XP_024304267.1:n.825+43T>A
XM_024448500.1:c.669+43T>A (ILK)	XP_024304268.1:n.669+43T>A
NM_006284.4:c.*1034A>T (TAF10) MANE Select	NP_006275.1:n.*1034A>T
NM_001014794.3:c.978+43T>A (ILK)	NP_001014794.1:n.978+43T>A
NM_001014795.3:c.978+43T>A (ILK)	NP_001014795.1:n.978+43T>A
NM_001278441.2:c.795+43T>A (ILK)	NP_001265370.1:n.795+43T>A
NM_004517.4:c.978+43T>A (ILK) MANE Select	NP_004508.1:n.978+43T>A
NM_001278442.2:c.576+43T>A (ILK)	NP_001265371.1:n.576+43T>A