Canonical Allele Identifier: CA1581041961

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833868_127833869delinsAC , CM000667.2:g.127833868_127833869delinsAC	GRCh38
NC_000005.9:g.127169560_127169561delinsAC , CM000667.1:g.127169560_127169561delinsAC	GRCh37
NC_000005.8:g.127197459_127197460delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35706_468+35707delinsAC	ENSP00000516662.1:n.468+35706_468+35707delinsAC
ENST00000514853.5:c.411+35706_411+35707delinsAC MANE Select	ENSP00000490579.2:n.411+35706_411+35707delinsAC
ENST00000514853.4:c.411+35706_411+35707delinsAC	ENSP00000490579.2:n.411+35706_411+35707delinsAC
XR_159059.3:n.500+35706_500+35707delinsAC
XR_246581.3:n.434+35706_434+35707delinsAC
XR_246582.2:n.366+35706_366+35707delinsAC
XR_948747.1:n.305-6451_305-6450delinsGT
XR_948748.1:n.396+35706_396+35707delinsAC
XR_948749.1:n.425+35706_425+35707delinsAC
XR_948750.1:n.593+35706_593+35707delinsAC
XR_948751.1:n.597+35706_597+35707delinsAC
XR_948752.1:n.316+35706_316+35707delinsAC
XR_948753.1:n.503+35706_503+35707delinsAC
XR_948754.1:n.502+35706_502+35707delinsAC
XR_948755.1:n.501+35706_501+35707delinsAC
XR_948756.1:n.501+35706_501+35707delinsAC
XR_948757.1:n.501+35706_501+35707delinsAC
XR_948758.1:n.501+35706_501+35707delinsAC
XR_948759.1:n.501+35706_501+35707delinsAC
XR_948761.1:n.521-15439_521-15438delinsAC
XR_948762.1:n.501+35706_501+35707delinsAC
XR_948764.1:n.502+35706_502+35707delinsAC
XR_948765.1:n.501+35706_501+35707delinsAC
XR_948766.1:n.502-4739_502-4738delinsAC
NM_001317938.1:c.468+35706_468+35707delinsAC	NP_001304867.1:n.468+35706_468+35707delinsAC
XM_017009805.1:c.381+35706_381+35707delinsAC	XP_016865294.1:n.381+35706_381+35707delinsAC
XM_017009806.2:c.348+35706_348+35707delinsAC	XP_016865295.1:n.348+35706_348+35707delinsAC
XM_017009807.1:c.348+35706_348+35707delinsAC	XP_016865296.1:n.348+35706_348+35707delinsAC
XM_017009808.1:c.306+35706_306+35707delinsAC	XP_016865297.1:n.306+35706_306+35707delinsAC
XM_017009809.2:c.468+35706_468+35707delinsAC	XP_016865298.1:n.468+35706_468+35707delinsAC
XM_017009810.2:c.468+35706_468+35707delinsAC	XP_016865299.1:n.468+35706_468+35707delinsAC
XM_017009811.2:c.468+35706_468+35707delinsAC	XP_016865300.1:n.468+35706_468+35707delinsAC
XM_017009812.2:c.468+35706_468+35707delinsAC	XP_016865301.1:n.468+35706_468+35707delinsAC
XM_017009813.2:c.469-4739_469-4738delinsAC	XP_016865302.1:n.469-4739_469-4738delinsAC
XM_024446203.1:c.348+35706_348+35707delinsAC	XP_024301971.1:n.348+35706_348+35707delinsAC
XR_002956177.1:n.434+35706_434+35707delinsAC
XR_948757.3:n.501+35706_501+35707delinsAC
NM_001317938.2:c.411+35706_411+35707delinsAC MANE Select	NP_001304867.2:n.411+35706_411+35707delinsAC