Canonical Allele Identifier: CA1581041952

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833856_127833857delinsCT , CM000667.2:g.127833856_127833857delinsCT	GRCh38
NC_000005.9:g.127169548_127169549delinsCT , CM000667.1:g.127169548_127169549delinsCT	GRCh37
NC_000005.8:g.127197447_127197448delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35694_468+35695delinsCT	ENSP00000516662.1:n.468+35694_468+35695delinsCT
ENST00000514853.5:c.411+35694_411+35695delinsCT MANE Select	ENSP00000490579.2:n.411+35694_411+35695delinsCT
ENST00000514853.4:c.411+35694_411+35695delinsCT	ENSP00000490579.2:n.411+35694_411+35695delinsCT
XR_159059.3:n.500+35694_500+35695delinsCT
XR_246581.3:n.434+35694_434+35695delinsCT
XR_246582.2:n.366+35694_366+35695delinsCT
XR_948747.1:n.305-6439_305-6438delinsAG
XR_948748.1:n.396+35694_396+35695delinsCT
XR_948749.1:n.425+35694_425+35695delinsCT
XR_948750.1:n.593+35694_593+35695delinsCT
XR_948751.1:n.597+35694_597+35695delinsCT
XR_948752.1:n.316+35694_316+35695delinsCT
XR_948753.1:n.503+35694_503+35695delinsCT
XR_948754.1:n.502+35694_502+35695delinsCT
XR_948755.1:n.501+35694_501+35695delinsCT
XR_948756.1:n.501+35694_501+35695delinsCT
XR_948757.1:n.501+35694_501+35695delinsCT
XR_948758.1:n.501+35694_501+35695delinsCT
XR_948759.1:n.501+35694_501+35695delinsCT
XR_948761.1:n.521-15451_521-15450delinsCT
XR_948762.1:n.501+35694_501+35695delinsCT
XR_948764.1:n.502+35694_502+35695delinsCT
XR_948765.1:n.501+35694_501+35695delinsCT
XR_948766.1:n.502-4751_502-4750delinsCT
NM_001317938.1:c.468+35694_468+35695delinsCT	NP_001304867.1:n.468+35694_468+35695delinsCT
XM_017009805.1:c.381+35694_381+35695delinsCT	XP_016865294.1:n.381+35694_381+35695delinsCT
XM_017009806.2:c.348+35694_348+35695delinsCT	XP_016865295.1:n.348+35694_348+35695delinsCT
XM_017009807.1:c.348+35694_348+35695delinsCT	XP_016865296.1:n.348+35694_348+35695delinsCT
XM_017009808.1:c.306+35694_306+35695delinsCT	XP_016865297.1:n.306+35694_306+35695delinsCT
XM_017009809.2:c.468+35694_468+35695delinsCT	XP_016865298.1:n.468+35694_468+35695delinsCT
XM_017009810.2:c.468+35694_468+35695delinsCT	XP_016865299.1:n.468+35694_468+35695delinsCT
XM_017009811.2:c.468+35694_468+35695delinsCT	XP_016865300.1:n.468+35694_468+35695delinsCT
XM_017009812.2:c.468+35694_468+35695delinsCT	XP_016865301.1:n.468+35694_468+35695delinsCT
XM_017009813.2:c.469-4751_469-4750delinsCT	XP_016865302.1:n.469-4751_469-4750delinsCT
XM_024446203.1:c.348+35694_348+35695delinsCT	XP_024301971.1:n.348+35694_348+35695delinsCT
XR_002956177.1:n.434+35694_434+35695delinsCT
XR_948757.3:n.501+35694_501+35695delinsCT
NM_001317938.2:c.411+35694_411+35695delinsCT MANE Select	NP_001304867.2:n.411+35694_411+35695delinsCT