Canonical Allele Identifier: CA2612255419

Gene: ILK TAF10

Linked Data

• gnomAD v4: 11-6609910-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6609913_6609915del , CM000673.2:g.6609913_6609915del	GRCh38
NC_000011.9:g.6631144_6631146del , CM000673.1:g.6631144_6631146del	GRCh37
NC_000011.8:g.6587720_6587722del	NCBI36
NG_029702.1:g.11181_11183del , LRG_444:g.11181_11183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299421.9:c.979-23_979-21del (ILK) MANE Select	ENSP00000299421.4:n.979-23_979-21del
ENST00000299424.9:c.*1009_*1011del (TAF10) MANE Select	ENSP00000299424.4:n.*1009_*1011del
ENST00000299421.8:c.979-23_979-21del (ILK)	ENSP00000299421.3:n.979-23_979-21del
ENST00000396751.6:c.979-23_979-21del (ILK)	ENSP00000379975.2:n.979-23_979-21del
ENST00000420936.6:c.979-23_979-21del (ILK)	ENSP00000403487.2:n.979-23_979-21del
ENST00000526318.2:c.328-690_328-688del (ILK)	ENSP00000480597.1:n.328-690_328-688del
ENST00000526711.5:c.*690-23_*690-21del (ILK)	ENSP00000479932.1:n.*690-23_*690-21del
ENST00000528784.5:n.852-23_852-21del (ILK)
ENST00000528995.5:c.796-23_796-21del (ILK)	ENSP00000435323.1:n.796-23_796-21del
ENST00000530016.5:n.1316-23_1316-21del (ILK)
ENST00000532063.5:c.577-23_577-21del (ILK)	ENSP00000434492.2:n.577-23_577-21del
ENST00000537806.5:c.1072-23_1072-21del (ILK)	ENSP00000439606.2:n.1072-23_1072-21del
ENST00000616342.1:n.1775_1777del (TAF10)
NM_001014794.2:c.979-23_979-21del (ILK)	NP_001014794.1:n.979-23_979-21del
NM_001014795.2:c.979-23_979-21del (ILK)	NP_001014795.1:n.979-23_979-21del
NM_001278441.1:c.796-23_796-21del (ILK)	NP_001265370.1:n.796-23_796-21del
NM_001278442.1:c.577-23_577-21del (ILK)	NP_001265371.1:n.577-23_577-21del
NM_004517.3:c.979-23_979-21del (ILK)	NP_004508.1:n.979-23_979-21del
XM_005252904.3:c.979-23_979-21del (ILK)	XP_005252961.1:n.979-23_979-21del
XM_005252905.1:c.577-23_577-21del (ILK)	XP_005252962.1:n.577-23_577-21del
XM_011520065.1:c.979-23_979-21del (ILK)	XP_011518367.1:n.979-23_979-21del
XM_005252904.5:c.979-23_979-21del (ILK)	XP_005252961.1:n.979-23_979-21del
XM_005252905.3:c.577-23_577-21del (ILK)	XP_005252962.1:n.577-23_577-21del
XM_017017672.1:c.826-23_826-21del (ILK)	XP_016873161.1:n.826-23_826-21del
XM_024448494.1:c.1072-23_1072-21del (ILK)	XP_024304262.1:n.1072-23_1072-21del
XM_024448495.1:c.1072-23_1072-21del (ILK)	XP_024304263.1:n.1072-23_1072-21del
XM_024448496.1:c.1072-23_1072-21del (ILK)	XP_024304264.1:n.1072-23_1072-21del
XM_024448497.1:c.1072-23_1072-21del (ILK)	XP_024304265.1:n.1072-23_1072-21del
XM_024448498.1:c.826-23_826-21del (ILK)	XP_024304266.1:n.826-23_826-21del
XM_024448499.1:c.826-23_826-21del (ILK)	XP_024304267.1:n.826-23_826-21del
XM_024448500.1:c.670-23_670-21del (ILK)	XP_024304268.1:n.670-23_670-21del
NM_006284.4:c.*1009_*1011del (TAF10) MANE Select	NP_006275.1:n.*1009_*1011del
NM_001014794.3:c.979-23_979-21del (ILK)	NP_001014794.1:n.979-23_979-21del
NM_001014795.3:c.979-23_979-21del (ILK)	NP_001014795.1:n.979-23_979-21del
NM_001278441.2:c.796-23_796-21del (ILK)	NP_001265370.1:n.796-23_796-21del
NM_004517.4:c.979-23_979-21del (ILK) MANE Select	NP_004508.1:n.979-23_979-21del
NM_001278442.2:c.577-23_577-21del (ILK)	NP_001265371.1:n.577-23_577-21del