Canonical Allele Identifier: CA1581041948

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833851_127833856delinsTTTCTC , CM000667.2:g.127833851_127833856delinsTTTCTC	GRCh38
NC_000005.9:g.127169543_127169548delinsTTTCTC , CM000667.1:g.127169543_127169548delinsTTTCTC	GRCh37
NC_000005.8:g.127197442_127197447delinsTTTCTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35689_468+35694delinsTTTCTC	ENSP00000516662.1:n.468+35689_468+35694delinsTTTCTC
ENST00000514853.5:c.411+35689_411+35694delinsTTTCTC MANE Select	ENSP00000490579.2:n.411+35689_411+35694delinsTTTCTC
ENST00000514853.4:c.411+35689_411+35694delinsTTTCTC	ENSP00000490579.2:n.411+35689_411+35694delinsTTTCTC
XR_159059.3:n.500+35689_500+35694delinsTTTCTC
XR_246581.3:n.434+35689_434+35694delinsTTTCTC
XR_246582.2:n.366+35689_366+35694delinsTTTCTC
XR_948747.1:n.305-6438_305-6433delinsGAGAAA
XR_948748.1:n.396+35689_396+35694delinsTTTCTC
XR_948749.1:n.425+35689_425+35694delinsTTTCTC
XR_948750.1:n.593+35689_593+35694delinsTTTCTC
XR_948751.1:n.597+35689_597+35694delinsTTTCTC
XR_948752.1:n.316+35689_316+35694delinsTTTCTC
XR_948753.1:n.503+35689_503+35694delinsTTTCTC
XR_948754.1:n.502+35689_502+35694delinsTTTCTC
XR_948755.1:n.501+35689_501+35694delinsTTTCTC
XR_948756.1:n.501+35689_501+35694delinsTTTCTC
XR_948757.1:n.501+35689_501+35694delinsTTTCTC
XR_948758.1:n.501+35689_501+35694delinsTTTCTC
XR_948759.1:n.501+35689_501+35694delinsTTTCTC
XR_948761.1:n.521-15456_521-15451delinsTTTCTC
XR_948762.1:n.501+35689_501+35694delinsTTTCTC
XR_948764.1:n.502+35689_502+35694delinsTTTCTC
XR_948765.1:n.501+35689_501+35694delinsTTTCTC
XR_948766.1:n.502-4756_502-4751delinsTTTCTC
NM_001317938.1:c.468+35689_468+35694delinsTTTCTC	NP_001304867.1:n.468+35689_468+35694delinsTTTCTC
XM_017009805.1:c.381+35689_381+35694delinsTTTCTC	XP_016865294.1:n.381+35689_381+35694delinsTTTCTC
XM_017009806.2:c.348+35689_348+35694delinsTTTCTC	XP_016865295.1:n.348+35689_348+35694delinsTTTCTC
XM_017009807.1:c.348+35689_348+35694delinsTTTCTC	XP_016865296.1:n.348+35689_348+35694delinsTTTCTC
XM_017009808.1:c.306+35689_306+35694delinsTTTCTC	XP_016865297.1:n.306+35689_306+35694delinsTTTCTC
XM_017009809.2:c.468+35689_468+35694delinsTTTCTC	XP_016865298.1:n.468+35689_468+35694delinsTTTCTC
XM_017009810.2:c.468+35689_468+35694delinsTTTCTC	XP_016865299.1:n.468+35689_468+35694delinsTTTCTC
XM_017009811.2:c.468+35689_468+35694delinsTTTCTC	XP_016865300.1:n.468+35689_468+35694delinsTTTCTC
XM_017009812.2:c.468+35689_468+35694delinsTTTCTC	XP_016865301.1:n.468+35689_468+35694delinsTTTCTC
XM_017009813.2:c.469-4756_469-4751delinsTTTCTC	XP_016865302.1:n.469-4756_469-4751delinsTTTCTC
XM_024446203.1:c.348+35689_348+35694delinsTTTCTC	XP_024301971.1:n.348+35689_348+35694delinsTTTCTC
XR_002956177.1:n.434+35689_434+35694delinsTTTCTC
XR_948757.3:n.501+35689_501+35694delinsTTTCTC
NM_001317938.2:c.411+35689_411+35694delinsTTTCTC MANE Select	NP_001304867.2:n.411+35689_411+35694delinsTTTCTC