Canonical Allele Identifier: CA1581041916

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833770_127833772delinsAAG , CM000667.2:g.127833770_127833772delinsAAG	GRCh38
NC_000005.9:g.127169462_127169464delinsAAG , CM000667.1:g.127169462_127169464delinsAAG	GRCh37
NC_000005.8:g.127197361_127197363delinsAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35608_468+35610delinsAAG	ENSP00000516662.1:n.468+35608_468+35610delinsAAG
ENST00000514853.5:c.411+35608_411+35610delinsAAG MANE Select	ENSP00000490579.2:n.411+35608_411+35610delinsAAG
ENST00000514853.4:c.411+35608_411+35610delinsAAG	ENSP00000490579.2:n.411+35608_411+35610delinsAAG
XR_159059.3:n.500+35608_500+35610delinsAAG
XR_246581.3:n.434+35608_434+35610delinsAAG
XR_246582.2:n.366+35608_366+35610delinsAAG
XR_948747.1:n.305-6354_305-6352delinsCTT
XR_948748.1:n.396+35608_396+35610delinsAAG
XR_948749.1:n.425+35608_425+35610delinsAAG
XR_948750.1:n.593+35608_593+35610delinsAAG
XR_948751.1:n.597+35608_597+35610delinsAAG
XR_948752.1:n.316+35608_316+35610delinsAAG
XR_948753.1:n.503+35608_503+35610delinsAAG
XR_948754.1:n.502+35608_502+35610delinsAAG
XR_948755.1:n.501+35608_501+35610delinsAAG
XR_948756.1:n.501+35608_501+35610delinsAAG
XR_948757.1:n.501+35608_501+35610delinsAAG
XR_948758.1:n.501+35608_501+35610delinsAAG
XR_948759.1:n.501+35608_501+35610delinsAAG
XR_948761.1:n.521-15537_521-15535delinsAAG
XR_948762.1:n.501+35608_501+35610delinsAAG
XR_948764.1:n.502+35608_502+35610delinsAAG
XR_948765.1:n.501+35608_501+35610delinsAAG
XR_948766.1:n.502-4837_502-4835delinsAAG
NM_001317938.1:c.468+35608_468+35610delinsAAG	NP_001304867.1:n.468+35608_468+35610delinsAAG
XM_017009805.1:c.381+35608_381+35610delinsAAG	XP_016865294.1:n.381+35608_381+35610delinsAAG
XM_017009806.2:c.348+35608_348+35610delinsAAG	XP_016865295.1:n.348+35608_348+35610delinsAAG
XM_017009807.1:c.348+35608_348+35610delinsAAG	XP_016865296.1:n.348+35608_348+35610delinsAAG
XM_017009808.1:c.306+35608_306+35610delinsAAG	XP_016865297.1:n.306+35608_306+35610delinsAAG
XM_017009809.2:c.468+35608_468+35610delinsAAG	XP_016865298.1:n.468+35608_468+35610delinsAAG
XM_017009810.2:c.468+35608_468+35610delinsAAG	XP_016865299.1:n.468+35608_468+35610delinsAAG
XM_017009811.2:c.468+35608_468+35610delinsAAG	XP_016865300.1:n.468+35608_468+35610delinsAAG
XM_017009812.2:c.468+35608_468+35610delinsAAG	XP_016865301.1:n.468+35608_468+35610delinsAAG
XM_017009813.2:c.469-4837_469-4835delinsAAG	XP_016865302.1:n.469-4837_469-4835delinsAAG
XM_024446203.1:c.348+35608_348+35610delinsAAG	XP_024301971.1:n.348+35608_348+35610delinsAAG
XR_002956177.1:n.434+35608_434+35610delinsAAG
XR_948757.3:n.501+35608_501+35610delinsAAG
NM_001317938.2:c.411+35608_411+35610delinsAAG MANE Select	NP_001304867.2:n.411+35608_411+35610delinsAAG