Canonical Allele Identifier: CA562885667

Gene: CCDC192

Linked Data

• dbSNP Id: rs1245911378
• gnomAD v2: 5-127169460-G-GCT
• gnomAD v3: 5-127833768-G-GCT
• gnomAD v4: 5-127833768-G-GCT
• MyVariant Identifiers: chr5:g.127169460_127169461insCT (hg19) ; chr5:g.127833768_127833769insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127833768_127833769insCT , CM000667.2:g.127833768_127833769insCT	GRCh38
NC_000005.9:g.127169460_127169461insCT , CM000667.1:g.127169460_127169461insCT	GRCh37
NC_000005.8:g.127197359_127197360insCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706942.1:c.468+35606_468+35607insCT	ENSP00000516662.1:n.468+35606_468+35607insCT
ENST00000514853.5:c.411+35606_411+35607insCT MANE Select	ENSP00000490579.2:n.411+35606_411+35607insCT
ENST00000514853.4:c.411+35606_411+35607insCT	ENSP00000490579.2:n.411+35606_411+35607insCT
XR_159059.3:n.500+35606_500+35607insCT
XR_246581.3:n.434+35606_434+35607insCT
XR_246582.2:n.366+35606_366+35607insCT
XR_948747.1:n.305-6351_305-6350insAG
XR_948748.1:n.396+35606_396+35607insCT
XR_948749.1:n.425+35606_425+35607insCT
XR_948750.1:n.593+35606_593+35607insCT
XR_948751.1:n.597+35606_597+35607insCT
XR_948752.1:n.316+35606_316+35607insCT
XR_948753.1:n.503+35606_503+35607insCT
XR_948754.1:n.502+35606_502+35607insCT
XR_948755.1:n.501+35606_501+35607insCT
XR_948756.1:n.501+35606_501+35607insCT
XR_948757.1:n.501+35606_501+35607insCT
XR_948758.1:n.501+35606_501+35607insCT
XR_948759.1:n.501+35606_501+35607insCT
XR_948761.1:n.521-15539_521-15538insCT
XR_948762.1:n.501+35606_501+35607insCT
XR_948764.1:n.502+35606_502+35607insCT
XR_948765.1:n.501+35606_501+35607insCT
XR_948766.1:n.502-4839_502-4838insCT
NM_001317938.1:c.468+35606_468+35607insCT	NP_001304867.1:n.468+35606_468+35607insCT
XM_017009805.1:c.381+35606_381+35607insCT	XP_016865294.1:n.381+35606_381+35607insCT
XM_017009806.2:c.348+35606_348+35607insCT	XP_016865295.1:n.348+35606_348+35607insCT
XM_017009807.1:c.348+35606_348+35607insCT	XP_016865296.1:n.348+35606_348+35607insCT
XM_017009808.1:c.306+35606_306+35607insCT	XP_016865297.1:n.306+35606_306+35607insCT
XM_017009809.2:c.468+35606_468+35607insCT	XP_016865298.1:n.468+35606_468+35607insCT
XM_017009810.2:c.468+35606_468+35607insCT	XP_016865299.1:n.468+35606_468+35607insCT
XM_017009811.2:c.468+35606_468+35607insCT	XP_016865300.1:n.468+35606_468+35607insCT
XM_017009812.2:c.468+35606_468+35607insCT	XP_016865301.1:n.468+35606_468+35607insCT
XM_017009813.2:c.469-4839_469-4838insCT	XP_016865302.1:n.469-4839_469-4838insCT
XM_024446203.1:c.348+35606_348+35607insCT	XP_024301971.1:n.348+35606_348+35607insCT
XR_002956177.1:n.434+35606_434+35607insCT
XR_948757.3:n.501+35606_501+35607insCT
NM_001317938.2:c.411+35606_411+35607insCT MANE Select	NP_001304867.2:n.411+35606_411+35607insCT