Canonical Allele Identifier: CA1581041885

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833707_127833708delinsGA , CM000667.2:g.127833707_127833708delinsGA	GRCh38
NC_000005.9:g.127169399_127169400delinsGA , CM000667.1:g.127169399_127169400delinsGA	GRCh37
NC_000005.8:g.127197298_127197299delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35545_468+35546delinsGA	ENSP00000516662.1:n.468+35545_468+35546delinsGA
ENST00000514853.5:c.411+35545_411+35546delinsGA MANE Select	ENSP00000490579.2:n.411+35545_411+35546delinsGA
ENST00000514853.4:c.411+35545_411+35546delinsGA	ENSP00000490579.2:n.411+35545_411+35546delinsGA
XR_159059.3:n.500+35545_500+35546delinsGA
XR_246581.3:n.434+35545_434+35546delinsGA
XR_246582.2:n.366+35545_366+35546delinsGA
XR_948747.1:n.305-6290_305-6289delinsTC
XR_948748.1:n.396+35545_396+35546delinsGA
XR_948749.1:n.425+35545_425+35546delinsGA
XR_948750.1:n.593+35545_593+35546delinsGA
XR_948751.1:n.597+35545_597+35546delinsGA
XR_948752.1:n.316+35545_316+35546delinsGA
XR_948753.1:n.503+35545_503+35546delinsGA
XR_948754.1:n.502+35545_502+35546delinsGA
XR_948755.1:n.501+35545_501+35546delinsGA
XR_948756.1:n.501+35545_501+35546delinsGA
XR_948757.1:n.501+35545_501+35546delinsGA
XR_948758.1:n.501+35545_501+35546delinsGA
XR_948759.1:n.501+35545_501+35546delinsGA
XR_948761.1:n.521-15600_521-15599delinsGA
XR_948762.1:n.501+35545_501+35546delinsGA
XR_948764.1:n.502+35545_502+35546delinsGA
XR_948765.1:n.501+35545_501+35546delinsGA
XR_948766.1:n.502-4900_502-4899delinsGA
NM_001317938.1:c.468+35545_468+35546delinsGA	NP_001304867.1:n.468+35545_468+35546delinsGA
XM_017009805.1:c.381+35545_381+35546delinsGA	XP_016865294.1:n.381+35545_381+35546delinsGA
XM_017009806.2:c.348+35545_348+35546delinsGA	XP_016865295.1:n.348+35545_348+35546delinsGA
XM_017009807.1:c.348+35545_348+35546delinsGA	XP_016865296.1:n.348+35545_348+35546delinsGA
XM_017009808.1:c.306+35545_306+35546delinsGA	XP_016865297.1:n.306+35545_306+35546delinsGA
XM_017009809.2:c.468+35545_468+35546delinsGA	XP_016865298.1:n.468+35545_468+35546delinsGA
XM_017009810.2:c.468+35545_468+35546delinsGA	XP_016865299.1:n.468+35545_468+35546delinsGA
XM_017009811.2:c.468+35545_468+35546delinsGA	XP_016865300.1:n.468+35545_468+35546delinsGA
XM_017009812.2:c.468+35545_468+35546delinsGA	XP_016865301.1:n.468+35545_468+35546delinsGA
XM_017009813.2:c.469-4900_469-4899delinsGA	XP_016865302.1:n.469-4900_469-4899delinsGA
XM_024446203.1:c.348+35545_348+35546delinsGA	XP_024301971.1:n.348+35545_348+35546delinsGA
XR_002956177.1:n.434+35545_434+35546delinsGA
XR_948757.3:n.501+35545_501+35546delinsGA
NM_001317938.2:c.411+35545_411+35546delinsGA MANE Select	NP_001304867.2:n.411+35545_411+35546delinsGA