Canonical Allele Identifier: CA1581041927

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833802_127833804delinsCTG , CM000667.2:g.127833802_127833804delinsCTG	GRCh38
NC_000005.9:g.127169494_127169496delinsCTG , CM000667.1:g.127169494_127169496delinsCTG	GRCh37
NC_000005.8:g.127197393_127197395delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35640_468+35642delinsCTG	ENSP00000516662.1:n.468+35640_468+35642delinsCTG
ENST00000514853.5:c.411+35640_411+35642delinsCTG MANE Select	ENSP00000490579.2:n.411+35640_411+35642delinsCTG
ENST00000514853.4:c.411+35640_411+35642delinsCTG	ENSP00000490579.2:n.411+35640_411+35642delinsCTG
XR_159059.3:n.500+35640_500+35642delinsCTG
XR_246581.3:n.434+35640_434+35642delinsCTG
XR_246582.2:n.366+35640_366+35642delinsCTG
XR_948747.1:n.305-6386_305-6384delinsCAG
XR_948748.1:n.396+35640_396+35642delinsCTG
XR_948749.1:n.425+35640_425+35642delinsCTG
XR_948750.1:n.593+35640_593+35642delinsCTG
XR_948751.1:n.597+35640_597+35642delinsCTG
XR_948752.1:n.316+35640_316+35642delinsCTG
XR_948753.1:n.503+35640_503+35642delinsCTG
XR_948754.1:n.502+35640_502+35642delinsCTG
XR_948755.1:n.501+35640_501+35642delinsCTG
XR_948756.1:n.501+35640_501+35642delinsCTG
XR_948757.1:n.501+35640_501+35642delinsCTG
XR_948758.1:n.501+35640_501+35642delinsCTG
XR_948759.1:n.501+35640_501+35642delinsCTG
XR_948761.1:n.521-15505_521-15503delinsCTG
XR_948762.1:n.501+35640_501+35642delinsCTG
XR_948764.1:n.502+35640_502+35642delinsCTG
XR_948765.1:n.501+35640_501+35642delinsCTG
XR_948766.1:n.502-4805_502-4803delinsCTG
NM_001317938.1:c.468+35640_468+35642delinsCTG	NP_001304867.1:n.468+35640_468+35642delinsCTG
XM_017009805.1:c.381+35640_381+35642delinsCTG	XP_016865294.1:n.381+35640_381+35642delinsCTG
XM_017009806.2:c.348+35640_348+35642delinsCTG	XP_016865295.1:n.348+35640_348+35642delinsCTG
XM_017009807.1:c.348+35640_348+35642delinsCTG	XP_016865296.1:n.348+35640_348+35642delinsCTG
XM_017009808.1:c.306+35640_306+35642delinsCTG	XP_016865297.1:n.306+35640_306+35642delinsCTG
XM_017009809.2:c.468+35640_468+35642delinsCTG	XP_016865298.1:n.468+35640_468+35642delinsCTG
XM_017009810.2:c.468+35640_468+35642delinsCTG	XP_016865299.1:n.468+35640_468+35642delinsCTG
XM_017009811.2:c.468+35640_468+35642delinsCTG	XP_016865300.1:n.468+35640_468+35642delinsCTG
XM_017009812.2:c.468+35640_468+35642delinsCTG	XP_016865301.1:n.468+35640_468+35642delinsCTG
XM_017009813.2:c.469-4805_469-4803delinsCTG	XP_016865302.1:n.469-4805_469-4803delinsCTG
XM_024446203.1:c.348+35640_348+35642delinsCTG	XP_024301971.1:n.348+35640_348+35642delinsCTG
XR_002956177.1:n.434+35640_434+35642delinsCTG
XR_948757.3:n.501+35640_501+35642delinsCTG
NM_001317938.2:c.411+35640_411+35642delinsCTG MANE Select	NP_001304867.2:n.411+35640_411+35642delinsCTG