Canonical Allele Identifier: CA5858237

Gene: ILK TAF10

Linked Data

• dbSNP Id: rs774886309
• ExAC: 11:6631101 C / CCCAGG
• gnomAD v2: 11-6631101-C-CCCAGG
• gnomAD v4: 11-6609870-C-CCCAGG
• MyVariant Identifiers: chr11:g.6631101_6631102insCCAGG (hg19) ; chr11:g.6609870_6609871insCCAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6609873_6609877dup , CM000673.2:g.6609873_6609877dup	GRCh38
NC_000011.9:g.6631104_6631108dup , CM000673.1:g.6631104_6631108dup	GRCh37
NC_000011.8:g.6587680_6587684dup	NCBI36
NG_029702.1:g.11141_11145dup , LRG_444:g.11141_11145dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299421.9:c.978+28_978+32dup (ILK) MANE Select	ENSP00000299421.4:n.978+28_978+32dup
ENST00000299424.9:c.*1047_*1051dup (TAF10) MANE Select	ENSP00000299424.4:n.*1047_*1051dup
ENST00000299421.8:c.978+28_978+32dup (ILK)	ENSP00000299421.3:n.978+28_978+32dup
ENST00000396751.6:c.978+28_978+32dup (ILK)	ENSP00000379975.2:n.978+28_978+32dup
ENST00000420936.6:c.978+28_978+32dup (ILK)	ENSP00000403487.2:n.978+28_978+32dup
ENST00000526318.2:c.328-730_328-726dup (ILK)	ENSP00000480597.1:n.328-730_328-726dup
ENST00000526711.5:c.*689+28_*689+32dup (ILK)	ENSP00000479932.1:n.*689+28_*689+32dup
ENST00000528784.5:n.851+28_851+32dup (ILK)
ENST00000528995.5:c.795+28_795+32dup (ILK)	ENSP00000435323.1:n.795+28_795+32dup
ENST00000530016.5:n.1315+28_1315+32dup (ILK)
ENST00000532063.5:c.576+28_576+32dup (ILK)	ENSP00000434492.2:n.576+28_576+32dup
ENST00000537806.5:c.1071+28_1071+32dup (ILK)	ENSP00000439606.2:n.1071+28_1071+32dup
ENST00000616342.1:n.1813_1817dup (TAF10)
NM_001014794.2:c.978+28_978+32dup (ILK)	NP_001014794.1:n.978+28_978+32dup
NM_001014795.2:c.978+28_978+32dup (ILK)	NP_001014795.1:n.978+28_978+32dup
NM_001278441.1:c.795+28_795+32dup (ILK)	NP_001265370.1:n.795+28_795+32dup
NM_001278442.1:c.576+28_576+32dup (ILK)	NP_001265371.1:n.576+28_576+32dup
NM_004517.3:c.978+28_978+32dup (ILK)	NP_004508.1:n.978+28_978+32dup
XM_005252904.3:c.978+28_978+32dup (ILK)	XP_005252961.1:n.978+28_978+32dup
XM_005252905.1:c.576+28_576+32dup (ILK)	XP_005252962.1:n.576+28_576+32dup
XM_011520065.1:c.978+28_978+32dup (ILK)	XP_011518367.1:n.978+28_978+32dup
XM_005252904.5:c.978+28_978+32dup (ILK)	XP_005252961.1:n.978+28_978+32dup
XM_005252905.3:c.576+28_576+32dup (ILK)	XP_005252962.1:n.576+28_576+32dup
XM_017017672.1:c.825+28_825+32dup (ILK)	XP_016873161.1:n.825+28_825+32dup
XM_024448494.1:c.1071+28_1071+32dup (ILK)	XP_024304262.1:n.1071+28_1071+32dup
XM_024448495.1:c.1071+28_1071+32dup (ILK)	XP_024304263.1:n.1071+28_1071+32dup
XM_024448496.1:c.1071+28_1071+32dup (ILK)	XP_024304264.1:n.1071+28_1071+32dup
XM_024448497.1:c.1071+28_1071+32dup (ILK)	XP_024304265.1:n.1071+28_1071+32dup
XM_024448498.1:c.825+28_825+32dup (ILK)	XP_024304266.1:n.825+28_825+32dup
XM_024448499.1:c.825+28_825+32dup (ILK)	XP_024304267.1:n.825+28_825+32dup
XM_024448500.1:c.669+28_669+32dup (ILK)	XP_024304268.1:n.669+28_669+32dup
NM_006284.4:c.*1047_*1051dup (TAF10) MANE Select	NP_006275.1:n.*1047_*1051dup
NM_001014794.3:c.978+28_978+32dup (ILK)	NP_001014794.1:n.978+28_978+32dup
NM_001014795.3:c.978+28_978+32dup (ILK)	NP_001014795.1:n.978+28_978+32dup
NM_001278441.2:c.795+28_795+32dup (ILK)	NP_001265370.1:n.795+28_795+32dup
NM_004517.4:c.978+28_978+32dup (ILK) MANE Select	NP_004508.1:n.978+28_978+32dup
NM_001278442.2:c.576+28_576+32dup (ILK)	NP_001265371.1:n.576+28_576+32dup