Canonical Allele Identifier: CA679357257

Gene: ILK TAF10

Linked Data

• dbSNP Id: rs1201765644
• MyVariant Identifiers: chr11:g.6631127_6631128insA (hg19) ; chr11:g.6609896_6609897insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6609896_6609897insA , CM000673.2:g.6609896_6609897insA	GRCh38
NC_000011.9:g.6631127_6631128insA , CM000673.1:g.6631127_6631128insA	GRCh37
NC_000011.8:g.6587703_6587704insA	NCBI36
NG_029702.1:g.11164_11165insA , LRG_444:g.11164_11165insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299421.9:c.979-40_979-39insA (ILK) MANE Select	ENSP00000299421.4:n.979-40_979-39insA
ENST00000299424.9:c.*1025_*1026insT (TAF10) MANE Select	ENSP00000299424.4:n.*1025_*1026insT
ENST00000299421.8:c.979-40_979-39insA (ILK)	ENSP00000299421.3:n.979-40_979-39insA
ENST00000396751.6:c.979-40_979-39insA (ILK)	ENSP00000379975.2:n.979-40_979-39insA
ENST00000420936.6:c.979-40_979-39insA (ILK)	ENSP00000403487.2:n.979-40_979-39insA
ENST00000526318.2:c.328-707_328-706insA (ILK)	ENSP00000480597.1:n.328-707_328-706insA
ENST00000526711.5:c.*690-40_*690-39insA (ILK)	ENSP00000479932.1:n.*690-40_*690-39insA
ENST00000528784.5:n.852-40_852-39insA (ILK)
ENST00000528995.5:c.796-40_796-39insA (ILK)	ENSP00000435323.1:n.796-40_796-39insA
ENST00000530016.5:n.1316-40_1316-39insA (ILK)
ENST00000532063.5:c.577-40_577-39insA (ILK)	ENSP00000434492.2:n.577-40_577-39insA
ENST00000537806.5:c.1072-40_1072-39insA (ILK)	ENSP00000439606.2:n.1072-40_1072-39insA
ENST00000616342.1:n.1791_1792insT (TAF10)
NM_001014794.2:c.979-40_979-39insA (ILK)	NP_001014794.1:n.979-40_979-39insA
NM_001014795.2:c.979-40_979-39insA (ILK)	NP_001014795.1:n.979-40_979-39insA
NM_001278441.1:c.796-40_796-39insA (ILK)	NP_001265370.1:n.796-40_796-39insA
NM_001278442.1:c.577-40_577-39insA (ILK)	NP_001265371.1:n.577-40_577-39insA
NM_004517.3:c.979-40_979-39insA (ILK)	NP_004508.1:n.979-40_979-39insA
XM_005252904.3:c.979-40_979-39insA (ILK)	XP_005252961.1:n.979-40_979-39insA
XM_005252905.1:c.577-40_577-39insA (ILK)	XP_005252962.1:n.577-40_577-39insA
XM_011520065.1:c.979-40_979-39insA (ILK)	XP_011518367.1:n.979-40_979-39insA
XM_005252904.5:c.979-40_979-39insA (ILK)	XP_005252961.1:n.979-40_979-39insA
XM_005252905.3:c.577-40_577-39insA (ILK)	XP_005252962.1:n.577-40_577-39insA
XM_017017672.1:c.826-40_826-39insA (ILK)	XP_016873161.1:n.826-40_826-39insA
XM_024448494.1:c.1072-40_1072-39insA (ILK)	XP_024304262.1:n.1072-40_1072-39insA
XM_024448495.1:c.1072-40_1072-39insA (ILK)	XP_024304263.1:n.1072-40_1072-39insA
XM_024448496.1:c.1072-40_1072-39insA (ILK)	XP_024304264.1:n.1072-40_1072-39insA
XM_024448497.1:c.1072-40_1072-39insA (ILK)	XP_024304265.1:n.1072-40_1072-39insA
XM_024448498.1:c.826-40_826-39insA (ILK)	XP_024304266.1:n.826-40_826-39insA
XM_024448499.1:c.826-40_826-39insA (ILK)	XP_024304267.1:n.826-40_826-39insA
XM_024448500.1:c.670-40_670-39insA (ILK)	XP_024304268.1:n.670-40_670-39insA
NM_006284.4:c.*1025_*1026insT (TAF10) MANE Select	NP_006275.1:n.*1025_*1026insT
NM_001014794.3:c.979-40_979-39insA (ILK)	NP_001014794.1:n.979-40_979-39insA
NM_001014795.3:c.979-40_979-39insA (ILK)	NP_001014795.1:n.979-40_979-39insA
NM_001278441.2:c.796-40_796-39insA (ILK)	NP_001265370.1:n.796-40_796-39insA
NM_004517.4:c.979-40_979-39insA (ILK) MANE Select	NP_004508.1:n.979-40_979-39insA
NM_001278442.2:c.577-40_577-39insA (ILK)	NP_001265371.1:n.577-40_577-39insA