Canonical Allele Identifier: CA1581041971

Gene: CCDC192

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833885_127833886delinsAT , CM000667.2:g.127833885_127833886delinsAT	GRCh38
NC_000005.9:g.127169577_127169578delinsAT , CM000667.1:g.127169577_127169578delinsAT	GRCh37
NC_000005.8:g.127197476_127197477delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35723_468+35724delinsAT	ENSP00000516662.1:n.468+35723_468+35724delinsAT
ENST00000514853.5:c.411+35723_411+35724delinsAT MANE Select	ENSP00000490579.2:n.411+35723_411+35724delinsAT
ENST00000514853.4:c.411+35723_411+35724delinsAT	ENSP00000490579.2:n.411+35723_411+35724delinsAT
XR_159059.3:n.500+35723_500+35724delinsAT
XR_246581.3:n.434+35723_434+35724delinsAT
XR_246582.2:n.366+35723_366+35724delinsAT
XR_948747.1:n.305-6468_305-6467delinsAT
XR_948748.1:n.396+35723_396+35724delinsAT
XR_948749.1:n.425+35723_425+35724delinsAT
XR_948750.1:n.593+35723_593+35724delinsAT
XR_948751.1:n.597+35723_597+35724delinsAT
XR_948752.1:n.316+35723_316+35724delinsAT
XR_948753.1:n.503+35723_503+35724delinsAT
XR_948754.1:n.502+35723_502+35724delinsAT
XR_948755.1:n.501+35723_501+35724delinsAT
XR_948756.1:n.501+35723_501+35724delinsAT
XR_948757.1:n.501+35723_501+35724delinsAT
XR_948758.1:n.501+35723_501+35724delinsAT
XR_948759.1:n.501+35723_501+35724delinsAT
XR_948761.1:n.521-15422_521-15421delinsAT
XR_948762.1:n.501+35723_501+35724delinsAT
XR_948764.1:n.502+35723_502+35724delinsAT
XR_948765.1:n.501+35723_501+35724delinsAT
XR_948766.1:n.502-4722_502-4721delinsAT
NM_001317938.1:c.468+35723_468+35724delinsAT	NP_001304867.1:n.468+35723_468+35724delinsAT
XM_017009805.1:c.381+35723_381+35724delinsAT	XP_016865294.1:n.381+35723_381+35724delinsAT
XM_017009806.2:c.348+35723_348+35724delinsAT	XP_016865295.1:n.348+35723_348+35724delinsAT
XM_017009807.1:c.348+35723_348+35724delinsAT	XP_016865296.1:n.348+35723_348+35724delinsAT
XM_017009808.1:c.306+35723_306+35724delinsAT	XP_016865297.1:n.306+35723_306+35724delinsAT
XM_017009809.2:c.468+35723_468+35724delinsAT	XP_016865298.1:n.468+35723_468+35724delinsAT
XM_017009810.2:c.468+35723_468+35724delinsAT	XP_016865299.1:n.468+35723_468+35724delinsAT
XM_017009811.2:c.468+35723_468+35724delinsAT	XP_016865300.1:n.468+35723_468+35724delinsAT
XM_017009812.2:c.468+35723_468+35724delinsAT	XP_016865301.1:n.468+35723_468+35724delinsAT
XM_017009813.2:c.469-4722_469-4721delinsAT	XP_016865302.1:n.469-4722_469-4721delinsAT
XM_024446203.1:c.348+35723_348+35724delinsAT	XP_024301971.1:n.348+35723_348+35724delinsAT
XR_002956177.1:n.434+35723_434+35724delinsAT
XR_948757.3:n.501+35723_501+35724delinsAT
NM_001317938.2:c.411+35723_411+35724delinsAT MANE Select	NP_001304867.2:n.411+35723_411+35724delinsAT