Canonical Allele Identifier: CA1581041967

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833883_127833887delinsCAATG , CM000667.2:g.127833883_127833887delinsCAATG	GRCh38
NC_000005.9:g.127169575_127169579delinsCAATG , CM000667.1:g.127169575_127169579delinsCAATG	GRCh37
NC_000005.8:g.127197474_127197478delinsCAATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35721_468+35725delinsCAATG	ENSP00000516662.1:n.468+35721_468+35725delinsCAATG
ENST00000514853.5:c.411+35721_411+35725delinsCAATG MANE Select	ENSP00000490579.2:n.411+35721_411+35725delinsCAATG
ENST00000514853.4:c.411+35721_411+35725delinsCAATG	ENSP00000490579.2:n.411+35721_411+35725delinsCAATG
XR_159059.3:n.500+35721_500+35725delinsCAATG
XR_246581.3:n.434+35721_434+35725delinsCAATG
XR_246582.2:n.366+35721_366+35725delinsCAATG
XR_948747.1:n.305-6469_305-6465delinsCATTG
XR_948748.1:n.396+35721_396+35725delinsCAATG
XR_948749.1:n.425+35721_425+35725delinsCAATG
XR_948750.1:n.593+35721_593+35725delinsCAATG
XR_948751.1:n.597+35721_597+35725delinsCAATG
XR_948752.1:n.316+35721_316+35725delinsCAATG
XR_948753.1:n.503+35721_503+35725delinsCAATG
XR_948754.1:n.502+35721_502+35725delinsCAATG
XR_948755.1:n.501+35721_501+35725delinsCAATG
XR_948756.1:n.501+35721_501+35725delinsCAATG
XR_948757.1:n.501+35721_501+35725delinsCAATG
XR_948758.1:n.501+35721_501+35725delinsCAATG
XR_948759.1:n.501+35721_501+35725delinsCAATG
XR_948761.1:n.521-15424_521-15420delinsCAATG
XR_948762.1:n.501+35721_501+35725delinsCAATG
XR_948764.1:n.502+35721_502+35725delinsCAATG
XR_948765.1:n.501+35721_501+35725delinsCAATG
XR_948766.1:n.502-4724_502-4720delinsCAATG
NM_001317938.1:c.468+35721_468+35725delinsCAATG	NP_001304867.1:n.468+35721_468+35725delinsCAATG
XM_017009805.1:c.381+35721_381+35725delinsCAATG	XP_016865294.1:n.381+35721_381+35725delinsCAATG
XM_017009806.2:c.348+35721_348+35725delinsCAATG	XP_016865295.1:n.348+35721_348+35725delinsCAATG
XM_017009807.1:c.348+35721_348+35725delinsCAATG	XP_016865296.1:n.348+35721_348+35725delinsCAATG
XM_017009808.1:c.306+35721_306+35725delinsCAATG	XP_016865297.1:n.306+35721_306+35725delinsCAATG
XM_017009809.2:c.468+35721_468+35725delinsCAATG	XP_016865298.1:n.468+35721_468+35725delinsCAATG
XM_017009810.2:c.468+35721_468+35725delinsCAATG	XP_016865299.1:n.468+35721_468+35725delinsCAATG
XM_017009811.2:c.468+35721_468+35725delinsCAATG	XP_016865300.1:n.468+35721_468+35725delinsCAATG
XM_017009812.2:c.468+35721_468+35725delinsCAATG	XP_016865301.1:n.468+35721_468+35725delinsCAATG
XM_017009813.2:c.469-4724_469-4720delinsCAATG	XP_016865302.1:n.469-4724_469-4720delinsCAATG
XM_024446203.1:c.348+35721_348+35725delinsCAATG	XP_024301971.1:n.348+35721_348+35725delinsCAATG
XR_002956177.1:n.434+35721_434+35725delinsCAATG
XR_948757.3:n.501+35721_501+35725delinsCAATG
NM_001317938.2:c.411+35721_411+35725delinsCAATG MANE Select	NP_001304867.2:n.411+35721_411+35725delinsCAATG