Canonical Allele Identifier: CA1581041979

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833898_127833899delinsAT , CM000667.2:g.127833898_127833899delinsAT	GRCh38
NC_000005.9:g.127169590_127169591delinsAT , CM000667.1:g.127169590_127169591delinsAT	GRCh37
NC_000005.8:g.127197489_127197490delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35736_468+35737delinsAT	ENSP00000516662.1:n.468+35736_468+35737delinsAT
ENST00000514853.5:c.411+35736_411+35737delinsAT MANE Select	ENSP00000490579.2:n.411+35736_411+35737delinsAT
ENST00000514853.4:c.411+35736_411+35737delinsAT	ENSP00000490579.2:n.411+35736_411+35737delinsAT
XR_159059.3:n.500+35736_500+35737delinsAT
XR_246581.3:n.434+35736_434+35737delinsAT
XR_246582.2:n.366+35736_366+35737delinsAT
XR_948747.1:n.305-6481_305-6480delinsAT
XR_948748.1:n.396+35736_396+35737delinsAT
XR_948749.1:n.425+35736_425+35737delinsAT
XR_948750.1:n.593+35736_593+35737delinsAT
XR_948751.1:n.597+35736_597+35737delinsAT
XR_948752.1:n.316+35736_316+35737delinsAT
XR_948753.1:n.503+35736_503+35737delinsAT
XR_948754.1:n.502+35736_502+35737delinsAT
XR_948755.1:n.501+35736_501+35737delinsAT
XR_948756.1:n.501+35736_501+35737delinsAT
XR_948757.1:n.501+35736_501+35737delinsAT
XR_948758.1:n.501+35736_501+35737delinsAT
XR_948759.1:n.501+35736_501+35737delinsAT
XR_948761.1:n.521-15409_521-15408delinsAT
XR_948762.1:n.501+35736_501+35737delinsAT
XR_948764.1:n.502+35736_502+35737delinsAT
XR_948765.1:n.501+35736_501+35737delinsAT
XR_948766.1:n.502-4709_502-4708delinsAT
NM_001317938.1:c.468+35736_468+35737delinsAT	NP_001304867.1:n.468+35736_468+35737delinsAT
XM_017009805.1:c.381+35736_381+35737delinsAT	XP_016865294.1:n.381+35736_381+35737delinsAT
XM_017009806.2:c.348+35736_348+35737delinsAT	XP_016865295.1:n.348+35736_348+35737delinsAT
XM_017009807.1:c.348+35736_348+35737delinsAT	XP_016865296.1:n.348+35736_348+35737delinsAT
XM_017009808.1:c.306+35736_306+35737delinsAT	XP_016865297.1:n.306+35736_306+35737delinsAT
XM_017009809.2:c.468+35736_468+35737delinsAT	XP_016865298.1:n.468+35736_468+35737delinsAT
XM_017009810.2:c.468+35736_468+35737delinsAT	XP_016865299.1:n.468+35736_468+35737delinsAT
XM_017009811.2:c.468+35736_468+35737delinsAT	XP_016865300.1:n.468+35736_468+35737delinsAT
XM_017009812.2:c.468+35736_468+35737delinsAT	XP_016865301.1:n.468+35736_468+35737delinsAT
XM_017009813.2:c.469-4709_469-4708delinsAT	XP_016865302.1:n.469-4709_469-4708delinsAT
XM_024446203.1:c.348+35736_348+35737delinsAT	XP_024301971.1:n.348+35736_348+35737delinsAT
XR_002956177.1:n.434+35736_434+35737delinsAT
XR_948757.3:n.501+35736_501+35737delinsAT
NM_001317938.2:c.411+35736_411+35737delinsAT MANE Select	NP_001304867.2:n.411+35736_411+35737delinsAT