Canonical Allele Identifier: CA1581041786

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833402_127833405delinsACTT , CM000667.2:g.127833402_127833405delinsACTT	GRCh38
NC_000005.9:g.127169094_127169097delinsACTT , CM000667.1:g.127169094_127169097delinsACTT	GRCh37
NC_000005.8:g.127196993_127196996delinsACTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35240_468+35243delinsACTT	ENSP00000516662.1:n.468+35240_468+35243delinsACTT
ENST00000514853.5:c.411+35240_411+35243delinsACTT MANE Select	ENSP00000490579.2:n.411+35240_411+35243delinsACTT
ENST00000514853.4:c.411+35240_411+35243delinsACTT	ENSP00000490579.2:n.411+35240_411+35243delinsACTT
XR_159059.3:n.500+35240_500+35243delinsACTT
XR_246581.3:n.434+35240_434+35243delinsACTT
XR_246582.2:n.366+35240_366+35243delinsACTT
XR_948747.1:n.305-5987_305-5984delinsAAGT
XR_948748.1:n.396+35240_396+35243delinsACTT
XR_948749.1:n.425+35240_425+35243delinsACTT
XR_948750.1:n.593+35240_593+35243delinsACTT
XR_948751.1:n.597+35240_597+35243delinsACTT
XR_948752.1:n.316+35240_316+35243delinsACTT
XR_948753.1:n.503+35240_503+35243delinsACTT
XR_948754.1:n.502+35240_502+35243delinsACTT
XR_948755.1:n.501+35240_501+35243delinsACTT
XR_948756.1:n.501+35240_501+35243delinsACTT
XR_948757.1:n.501+35240_501+35243delinsACTT
XR_948758.1:n.501+35240_501+35243delinsACTT
XR_948759.1:n.501+35240_501+35243delinsACTT
XR_948761.1:n.521-15905_521-15902delinsACTT
XR_948762.1:n.501+35240_501+35243delinsACTT
XR_948764.1:n.502+35240_502+35243delinsACTT
XR_948765.1:n.501+35240_501+35243delinsACTT
XR_948766.1:n.502-5205_502-5202delinsACTT
NM_001317938.1:c.468+35240_468+35243delinsACTT	NP_001304867.1:n.468+35240_468+35243delinsACTT
XM_017009805.1:c.381+35240_381+35243delinsACTT	XP_016865294.1:n.381+35240_381+35243delinsACTT
XM_017009806.2:c.348+35240_348+35243delinsACTT	XP_016865295.1:n.348+35240_348+35243delinsACTT
XM_017009807.1:c.348+35240_348+35243delinsACTT	XP_016865296.1:n.348+35240_348+35243delinsACTT
XM_017009808.1:c.306+35240_306+35243delinsACTT	XP_016865297.1:n.306+35240_306+35243delinsACTT
XM_017009809.2:c.468+35240_468+35243delinsACTT	XP_016865298.1:n.468+35240_468+35243delinsACTT
XM_017009810.2:c.468+35240_468+35243delinsACTT	XP_016865299.1:n.468+35240_468+35243delinsACTT
XM_017009811.2:c.468+35240_468+35243delinsACTT	XP_016865300.1:n.468+35240_468+35243delinsACTT
XM_017009812.2:c.468+35240_468+35243delinsACTT	XP_016865301.1:n.468+35240_468+35243delinsACTT
XM_017009813.2:c.469-5205_469-5202delinsACTT	XP_016865302.1:n.469-5205_469-5202delinsACTT
XM_024446203.1:c.348+35240_348+35243delinsACTT	XP_024301971.1:n.348+35240_348+35243delinsACTT
XR_002956177.1:n.434+35240_434+35243delinsACTT
XR_948757.3:n.501+35240_501+35243delinsACTT
NM_001317938.2:c.411+35240_411+35243delinsACTT MANE Select	NP_001304867.2:n.411+35240_411+35243delinsACTT