Canonical Allele Identifier: CA1581041745

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833284_127833287delinsATCT , CM000667.2:g.127833284_127833287delinsATCT	GRCh38
NC_000005.9:g.127168976_127168979delinsATCT , CM000667.1:g.127168976_127168979delinsATCT	GRCh37
NC_000005.8:g.127196875_127196878delinsATCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35122_468+35125delinsATCT	ENSP00000516662.1:n.468+35122_468+35125delinsATCT
ENST00000514853.5:c.411+35122_411+35125delinsATCT MANE Select	ENSP00000490579.2:n.411+35122_411+35125delinsATCT
ENST00000514853.4:c.411+35122_411+35125delinsATCT	ENSP00000490579.2:n.411+35122_411+35125delinsATCT
XR_159059.3:n.500+35122_500+35125delinsATCT
XR_246581.3:n.434+35122_434+35125delinsATCT
XR_246582.2:n.366+35122_366+35125delinsATCT
XR_948747.1:n.305-5869_305-5866delinsAGAT
XR_948748.1:n.396+35122_396+35125delinsATCT
XR_948749.1:n.425+35122_425+35125delinsATCT
XR_948750.1:n.593+35122_593+35125delinsATCT
XR_948751.1:n.597+35122_597+35125delinsATCT
XR_948752.1:n.316+35122_316+35125delinsATCT
XR_948753.1:n.503+35122_503+35125delinsATCT
XR_948754.1:n.502+35122_502+35125delinsATCT
XR_948755.1:n.501+35122_501+35125delinsATCT
XR_948756.1:n.501+35122_501+35125delinsATCT
XR_948757.1:n.501+35122_501+35125delinsATCT
XR_948758.1:n.501+35122_501+35125delinsATCT
XR_948759.1:n.501+35122_501+35125delinsATCT
XR_948761.1:n.521-16023_521-16020delinsATCT
XR_948762.1:n.501+35122_501+35125delinsATCT
XR_948764.1:n.502+35122_502+35125delinsATCT
XR_948765.1:n.501+35122_501+35125delinsATCT
XR_948766.1:n.502-5323_502-5320delinsATCT
NM_001317938.1:c.468+35122_468+35125delinsATCT	NP_001304867.1:n.468+35122_468+35125delinsATCT
XM_017009805.1:c.381+35122_381+35125delinsATCT	XP_016865294.1:n.381+35122_381+35125delinsATCT
XM_017009806.2:c.348+35122_348+35125delinsATCT	XP_016865295.1:n.348+35122_348+35125delinsATCT
XM_017009807.1:c.348+35122_348+35125delinsATCT	XP_016865296.1:n.348+35122_348+35125delinsATCT
XM_017009808.1:c.306+35122_306+35125delinsATCT	XP_016865297.1:n.306+35122_306+35125delinsATCT
XM_017009809.2:c.468+35122_468+35125delinsATCT	XP_016865298.1:n.468+35122_468+35125delinsATCT
XM_017009810.2:c.468+35122_468+35125delinsATCT	XP_016865299.1:n.468+35122_468+35125delinsATCT
XM_017009811.2:c.468+35122_468+35125delinsATCT	XP_016865300.1:n.468+35122_468+35125delinsATCT
XM_017009812.2:c.468+35122_468+35125delinsATCT	XP_016865301.1:n.468+35122_468+35125delinsATCT
XM_017009813.2:c.469-5323_469-5320delinsATCT	XP_016865302.1:n.469-5323_469-5320delinsATCT
XM_024446203.1:c.348+35122_348+35125delinsATCT	XP_024301971.1:n.348+35122_348+35125delinsATCT
XR_002956177.1:n.434+35122_434+35125delinsATCT
XR_948757.3:n.501+35122_501+35125delinsATCT
NM_001317938.2:c.411+35122_411+35125delinsATCT MANE Select	NP_001304867.2:n.411+35122_411+35125delinsATCT