Canonical Allele Identifier: CA1950225381

Gene: ILK TAF10

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6610045_6610048delinsGTCA , CM000673.2:g.6610045_6610048delinsGTCA	GRCh38
NC_000011.9:g.6631276_6631279delinsGTCA , CM000673.1:g.6631276_6631279delinsGTCA	GRCh37
NC_000011.8:g.6587852_6587855delinsGTCA	NCBI36
NG_029702.1:g.11313_11316delinsGTCA , LRG_444:g.11313_11316delinsGTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299421.9:c.1078+10_1078+13delinsGTCA (ILK) MANE Select	ENSP00000299421.4:n.1078+10_1078+13delinsGTCA
ENST00000299424.9:c.*874_*877delinsTGAC (TAF10) MANE Select	ENSP00000299424.4:n.*874_*877delinsTGAC
ENST00000299421.8:c.1078+10_1078+13delinsGTCA (ILK)	ENSP00000299421.3:n.1078+10_1078+13delinsGTCA
ENST00000396751.6:c.1078+10_1078+13delinsGTCA (ILK)	ENSP00000379975.2:n.1078+10_1078+13delinsGTCA
ENST00000420936.6:c.1078+10_1078+13delinsGTCA (ILK)	ENSP00000403487.2:n.1078+10_1078+13delinsGTCA
ENST00000526318.2:c.328-558_328-555delinsGTCA (ILK)	ENSP00000480597.1:n.328-558_328-555delinsGTCA
ENST00000526711.5:c.*789+10_*789+13delinsGTCA (ILK)	ENSP00000479932.1:n.*789+10_*789+13delinsGTCA
ENST00000528995.5:c.895+10_895+13delinsGTCA (ILK)	ENSP00000435323.1:n.895+10_895+13delinsGTCA
ENST00000530016.5:n.1415+10_1415+13delinsGTCA (ILK)
ENST00000532063.5:c.676+10_676+13delinsGTCA (ILK)	ENSP00000434492.2:n.676+10_676+13delinsGTCA
ENST00000537806.5:c.1171+10_1171+13delinsGTCA (ILK)	ENSP00000439606.2:n.1171+10_1171+13delinsGTCA
ENST00000616342.1:n.1640_1643delinsTGAC (TAF10)
NM_001014794.2:c.1078+10_1078+13delinsGTCA (ILK)	NP_001014794.1:n.1078+10_1078+13delinsGTCA
NM_001014795.2:c.1078+10_1078+13delinsGTCA (ILK)	NP_001014795.1:n.1078+10_1078+13delinsGTCA
NM_001278441.1:c.895+10_895+13delinsGTCA (ILK)	NP_001265370.1:n.895+10_895+13delinsGTCA
NM_001278442.1:c.676+10_676+13delinsGTCA (ILK)	NP_001265371.1:n.676+10_676+13delinsGTCA
NM_004517.3:c.1078+10_1078+13delinsGTCA (ILK)	NP_004508.1:n.1078+10_1078+13delinsGTCA
XM_005252904.3:c.1078+10_1078+13delinsGTCA (ILK)	XP_005252961.1:n.1078+10_1078+13delinsGTCA
XM_005252905.1:c.676+10_676+13delinsGTCA (ILK)	XP_005252962.1:n.676+10_676+13delinsGTCA
XM_011520065.1:c.1078+10_1078+13delinsGTCA (ILK)	XP_011518367.1:n.1078+10_1078+13delinsGTCA
XM_005252904.5:c.1078+10_1078+13delinsGTCA (ILK)	XP_005252961.1:n.1078+10_1078+13delinsGTCA
XM_005252905.3:c.676+10_676+13delinsGTCA (ILK)	XP_005252962.1:n.676+10_676+13delinsGTCA
XM_017017672.1:c.925+10_925+13delinsGTCA (ILK)	XP_016873161.1:n.925+10_925+13delinsGTCA
XM_024448494.1:c.1171+10_1171+13delinsGTCA (ILK)	XP_024304262.1:n.1171+10_1171+13delinsGTCA
XM_024448495.1:c.1171+10_1171+13delinsGTCA (ILK)	XP_024304263.1:n.1171+10_1171+13delinsGTCA
XM_024448496.1:c.1171+10_1171+13delinsGTCA (ILK)	XP_024304264.1:n.1171+10_1171+13delinsGTCA
XM_024448497.1:c.1171+10_1171+13delinsGTCA (ILK)	XP_024304265.1:n.1171+10_1171+13delinsGTCA
XM_024448498.1:c.925+10_925+13delinsGTCA (ILK)	XP_024304266.1:n.925+10_925+13delinsGTCA
XM_024448499.1:c.925+10_925+13delinsGTCA (ILK)	XP_024304267.1:n.925+10_925+13delinsGTCA
XM_024448500.1:c.769+10_769+13delinsGTCA (ILK)	XP_024304268.1:n.769+10_769+13delinsGTCA
NM_006284.4:c.*874_*877delinsTGAC (TAF10) MANE Select	NP_006275.1:n.*874_*877delinsTGAC
NM_001014794.3:c.1078+10_1078+13delinsGTCA (ILK)	NP_001014794.1:n.1078+10_1078+13delinsGTCA
NM_001014795.3:c.1078+10_1078+13delinsGTCA (ILK)	NP_001014795.1:n.1078+10_1078+13delinsGTCA
NM_001278441.2:c.895+10_895+13delinsGTCA (ILK)	NP_001265370.1:n.895+10_895+13delinsGTCA
NM_004517.4:c.1078+10_1078+13delinsGTCA (ILK) MANE Select	NP_004508.1:n.1078+10_1078+13delinsGTCA
NM_001278442.2:c.676+10_676+13delinsGTCA (ILK)	NP_001265371.1:n.676+10_676+13delinsGTCA