Canonical Allele Identifier: CA1581041926

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833800_127833802delinsTTC , CM000667.2:g.127833800_127833802delinsTTC	GRCh38
NC_000005.9:g.127169492_127169494delinsTTC , CM000667.1:g.127169492_127169494delinsTTC	GRCh37
NC_000005.8:g.127197391_127197393delinsTTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35638_468+35640delinsTTC	ENSP00000516662.1:n.468+35638_468+35640delinsTTC
ENST00000514853.5:c.411+35638_411+35640delinsTTC MANE Select	ENSP00000490579.2:n.411+35638_411+35640delinsTTC
ENST00000514853.4:c.411+35638_411+35640delinsTTC	ENSP00000490579.2:n.411+35638_411+35640delinsTTC
XR_159059.3:n.500+35638_500+35640delinsTTC
XR_246581.3:n.434+35638_434+35640delinsTTC
XR_246582.2:n.366+35638_366+35640delinsTTC
XR_948747.1:n.305-6384_305-6382delinsGAA
XR_948748.1:n.396+35638_396+35640delinsTTC
XR_948749.1:n.425+35638_425+35640delinsTTC
XR_948750.1:n.593+35638_593+35640delinsTTC
XR_948751.1:n.597+35638_597+35640delinsTTC
XR_948752.1:n.316+35638_316+35640delinsTTC
XR_948753.1:n.503+35638_503+35640delinsTTC
XR_948754.1:n.502+35638_502+35640delinsTTC
XR_948755.1:n.501+35638_501+35640delinsTTC
XR_948756.1:n.501+35638_501+35640delinsTTC
XR_948757.1:n.501+35638_501+35640delinsTTC
XR_948758.1:n.501+35638_501+35640delinsTTC
XR_948759.1:n.501+35638_501+35640delinsTTC
XR_948761.1:n.521-15507_521-15505delinsTTC
XR_948762.1:n.501+35638_501+35640delinsTTC
XR_948764.1:n.502+35638_502+35640delinsTTC
XR_948765.1:n.501+35638_501+35640delinsTTC
XR_948766.1:n.502-4807_502-4805delinsTTC
NM_001317938.1:c.468+35638_468+35640delinsTTC	NP_001304867.1:n.468+35638_468+35640delinsTTC
XM_017009805.1:c.381+35638_381+35640delinsTTC	XP_016865294.1:n.381+35638_381+35640delinsTTC
XM_017009806.2:c.348+35638_348+35640delinsTTC	XP_016865295.1:n.348+35638_348+35640delinsTTC
XM_017009807.1:c.348+35638_348+35640delinsTTC	XP_016865296.1:n.348+35638_348+35640delinsTTC
XM_017009808.1:c.306+35638_306+35640delinsTTC	XP_016865297.1:n.306+35638_306+35640delinsTTC
XM_017009809.2:c.468+35638_468+35640delinsTTC	XP_016865298.1:n.468+35638_468+35640delinsTTC
XM_017009810.2:c.468+35638_468+35640delinsTTC	XP_016865299.1:n.468+35638_468+35640delinsTTC
XM_017009811.2:c.468+35638_468+35640delinsTTC	XP_016865300.1:n.468+35638_468+35640delinsTTC
XM_017009812.2:c.468+35638_468+35640delinsTTC	XP_016865301.1:n.468+35638_468+35640delinsTTC
XM_017009813.2:c.469-4807_469-4805delinsTTC	XP_016865302.1:n.469-4807_469-4805delinsTTC
XM_024446203.1:c.348+35638_348+35640delinsTTC	XP_024301971.1:n.348+35638_348+35640delinsTTC
XR_002956177.1:n.434+35638_434+35640delinsTTC
XR_948757.3:n.501+35638_501+35640delinsTTC
NM_001317938.2:c.411+35638_411+35640delinsTTC MANE Select	NP_001304867.2:n.411+35638_411+35640delinsTTC