Canonical Allele Identifier: CA1950223626

Gene: ILK TAF10

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6608801C>G , CM000673.2:g.6608801C>G	GRCh38
NC_000011.9:g.6630032C>G , CM000673.1:g.6630032C>G	GRCh37
NC_000011.8:g.6586608C>G	NCBI36
NG_029702.1:g.10069C>G , LRG_444:g.10069C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299421.9:c.448+11C>G (ILK) MANE Select	ENSP00000299421.4:n.448+11C>G
ENST00000299424.9:c.*2121G>C (TAF10) MANE Select	ENSP00000299424.4:n.*2121G>C
ENST00000299421.8:c.448+11C>G (ILK)	ENSP00000299421.3:n.448+11C>G
ENST00000396751.6:c.448+11C>G (ILK)	ENSP00000379975.2:n.448+11C>G
ENST00000420936.6:c.448+11C>G (ILK)	ENSP00000403487.2:n.448+11C>G
ENST00000526114.5:c.*428+11C>G (ILK)	ENSP00000432617.1:n.*428+11C>G
ENST00000526318.2:c.327+312C>G (ILK)	ENSP00000480597.1:n.327+312C>G
ENST00000526711.5:c.*159+11C>G (ILK)	ENSP00000479932.1:n.*159+11C>G
ENST00000527121.5:c.*428+11C>G (ILK)	ENSP00000436062.1:n.*428+11C>G
ENST00000528784.5:n.321+11C>G (ILK)
ENST00000528995.5:c.352-83C>G (ILK)	ENSP00000435323.1:n.352-83C>G
ENST00000530016.5:n.600C>G (ILK)
ENST00000532063.5:c.46+11C>G (ILK)	ENSP00000434492.2:n.46+11C>G
ENST00000534706.1:n.45+11C>G (ILK)
ENST00000537806.5:c.459C>G (ILK)	ENSP00000439606.2:p.Pro153=
ENST00000616342.1:n.2887G>C (TAF10)
NM_001014794.2:c.448+11C>G (ILK)	NP_001014794.1:n.448+11C>G
NM_001014795.2:c.448+11C>G (ILK)	NP_001014795.1:n.448+11C>G
NM_001278441.1:c.352-83C>G (ILK)	NP_001265370.1:n.352-83C>G
NM_001278442.1:c.46+11C>G (ILK)	NP_001265371.1:n.46+11C>G
NM_004517.3:c.448+11C>G (ILK)	NP_004508.1:n.448+11C>G
XM_005252904.3:c.448+11C>G (ILK)	XP_005252961.1:n.448+11C>G
XM_005252905.1:c.46+11C>G (ILK)	XP_005252962.1:n.46+11C>G
XM_011520065.1:c.448+11C>G (ILK)	XP_011518367.1:n.448+11C>G
XM_005252904.5:c.448+11C>G (ILK)	XP_005252961.1:n.448+11C>G
XM_005252905.3:c.46+11C>G (ILK)	XP_005252962.1:n.46+11C>G
XM_017017672.1:c.295+11C>G (ILK)	XP_016873161.1:n.295+11C>G
XM_024448494.1:c.459C>G (ILK)	XP_024304262.1:p.Pro153=
XM_024448495.1:c.459C>G (ILK)	XP_024304263.1:p.Pro153=
XM_024448496.1:c.459C>G (ILK)	XP_024304264.1:p.Pro153=
XM_024448497.1:c.459C>G (ILK)	XP_024304265.1:p.Pro153=
XM_024448498.1:c.295+11C>G (ILK)	XP_024304266.1:n.295+11C>G
XM_024448499.1:c.295+11C>G (ILK)	XP_024304267.1:n.295+11C>G
XM_024448500.1:c.57C>G (ILK)	XP_024304268.1:p.Pro19=
NM_006284.4:c.*2121G>C (TAF10) MANE Select	NP_006275.1:n.*2121G>C
NM_001014794.3:c.448+11C>G (ILK)	NP_001014794.1:n.448+11C>G
NM_001014795.3:c.448+11C>G (ILK)	NP_001014795.1:n.448+11C>G
NM_001278441.2:c.352-83C>G (ILK)	NP_001265370.1:n.352-83C>G
NM_004517.4:c.448+11C>G (ILK) MANE Select	NP_004508.1:n.448+11C>G
NM_001278442.2:c.46+11C>G (ILK)	NP_001265371.1:n.46+11C>G