Canonical Allele Identifier: CA1081326671

Gene: CCDC192

Linked Data

• dbSNP Id: rs1749915349
• gnomAD v3: 5-127833883-CAATG-C
• gnomAD v4: 5-127833883-CAATG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833884_127833887del , CM000667.2:g.127833884_127833887del	GRCh38
NC_000005.9:g.127169576_127169579del , CM000667.1:g.127169576_127169579del	GRCh37
NC_000005.8:g.127197475_127197478del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35722_468+35725del	ENSP00000516662.1:n.468+35722_468+35725del
ENST00000514853.5:c.411+35722_411+35725del MANE Select	ENSP00000490579.2:n.411+35722_411+35725del
ENST00000514853.4:c.411+35722_411+35725del	ENSP00000490579.2:n.411+35722_411+35725del
XR_159059.3:n.500+35722_500+35725del
XR_246581.3:n.434+35722_434+35725del
XR_246582.2:n.366+35722_366+35725del
XR_948747.1:n.305-6469_305-6466del
XR_948748.1:n.396+35722_396+35725del
XR_948749.1:n.425+35722_425+35725del
XR_948750.1:n.593+35722_593+35725del
XR_948751.1:n.597+35722_597+35725del
XR_948752.1:n.316+35722_316+35725del
XR_948753.1:n.503+35722_503+35725del
XR_948754.1:n.502+35722_502+35725del
XR_948755.1:n.501+35722_501+35725del
XR_948756.1:n.501+35722_501+35725del
XR_948757.1:n.501+35722_501+35725del
XR_948758.1:n.501+35722_501+35725del
XR_948759.1:n.501+35722_501+35725del
XR_948761.1:n.521-15423_521-15420del
XR_948762.1:n.501+35722_501+35725del
XR_948764.1:n.502+35722_502+35725del
XR_948765.1:n.501+35722_501+35725del
XR_948766.1:n.502-4723_502-4720del
NM_001317938.1:c.468+35722_468+35725del	NP_001304867.1:n.468+35722_468+35725del
XM_017009805.1:c.381+35722_381+35725del	XP_016865294.1:n.381+35722_381+35725del
XM_017009806.2:c.348+35722_348+35725del	XP_016865295.1:n.348+35722_348+35725del
XM_017009807.1:c.348+35722_348+35725del	XP_016865296.1:n.348+35722_348+35725del
XM_017009808.1:c.306+35722_306+35725del	XP_016865297.1:n.306+35722_306+35725del
XM_017009809.2:c.468+35722_468+35725del	XP_016865298.1:n.468+35722_468+35725del
XM_017009810.2:c.468+35722_468+35725del	XP_016865299.1:n.468+35722_468+35725del
XM_017009811.2:c.468+35722_468+35725del	XP_016865300.1:n.468+35722_468+35725del
XM_017009812.2:c.468+35722_468+35725del	XP_016865301.1:n.468+35722_468+35725del
XM_017009813.2:c.469-4723_469-4720del	XP_016865302.1:n.469-4723_469-4720del
XM_024446203.1:c.348+35722_348+35725del	XP_024301971.1:n.348+35722_348+35725del
XR_002956177.1:n.434+35722_434+35725del
XR_948757.3:n.501+35722_501+35725del
NM_001317938.2:c.411+35722_411+35725del MANE Select	NP_001304867.2:n.411+35722_411+35725del