Canonical Allele Identifier: CA2679782452

Gene: CCNC TSTD3

Linked Data

• gnomAD v4: 6-99558429-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.99558429_99558430insG , CM000668.2:g.99558429_99558430insG	GRCh38
NC_000006.11:g.100006305_100006306insG , CM000668.1:g.100006305_100006306insG	GRCh37
NC_000006.10:g.100113026_100113027insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000520429.6:c.346+67_346+68insC (CCNC) MANE Select	ENSP00000428982.1:n.346+67_346+68insC
ENST00000607332.2:n.552-9137_552-9136insG (TSTD3)
ENST00000623858.2:n.552-26451_552-26450insG (TSTD3)
ENST00000651400.1:n.336-17224_336-17223insG (TSTD3)
ENST00000326298.8:c.346+67_346+68insC (CCNC)	ENSP00000319027.4:n.346+67_346+68insC
ENST00000369217.8:c.487+67_487+68insC (CCNC)	ENSP00000428472.1:n.487+67_487+68insC
ENST00000369220.8:c.346+67_346+68insC (CCNC)	ENSP00000358222.4:n.346+67_346+68insC
ENST00000482541.2:c.413_414insC (CCNC)	ENSP00000417072.2:p.Ser142Ter
ENST00000484049.6:c.342+71_342+72insC (CCNC)	ENSP00000430718.1:n.342+71_342+72insC
ENST00000486428.6:c.184+67_184+68insC (CCNC)	ENSP00000430077.1:n.184+67_184+68insC
ENST00000518714.5:c.346+67_346+68insC (CCNC)	ENSP00000430294.1:n.346+67_346+68insC
ENST00000520371.5:c.346+67_346+68insC (CCNC)	ENSP00000430381.1:n.346+67_346+68insC
ENST00000520429.5:c.346+67_346+68insC (CCNC)	ENSP00000428982.1:n.346+67_346+68insC
ENST00000521017.5:n.447+67_447+68insC (CCNC)
ENST00000523310.1:n.465_466insC (CCNC)
ENST00000523639.5:n.586+67_586+68insC (CCNC)
ENST00000523799.5:c.91+67_91+68insC (CCNC)	ENSP00000430014.1:n.91+67_91+68insC
ENST00000523961.5:c.*111+67_*111+68insC (CCNC)	ENSP00000428577.1:n.*111+67_*111+68insC
ENST00000523985.5:c.91+67_91+68insC (CCNC)	ENSP00000430119.1:n.91+67_91+68insC
ENST00000524049.5:c.91+67_91+68insC (CCNC)	ENSP00000427885.1:n.91+67_91+68insC
ENST00000627680.2:c.346+67_346+68insC (CCNC)	ENSP00000487040.1:n.346+67_346+68insC
NM_001013399.1:c.91+67_91+68insC (CCNC)	NP_001013417.1:n.91+67_91+68insC
NM_005190.3:c.346+67_346+68insC (CCNC)	NP_005181.2:n.346+67_346+68insC
XM_006715594.1:c.346+67_346+68insC (CCNC)	XP_006715657.1:n.346+67_346+68insC
XM_011536232.1:c.346+67_346+68insC (CCNC)	XP_011534534.1:n.346+67_346+68insC
XR_942234.1:n.701-20033_701-20032insG (TSTD3)
NM_001363537.1:c.346+67_346+68insC (CCNC)	NP_001350466.1:n.346+67_346+68insC
XM_011536232.3:c.346+67_346+68insC (CCNC)	XP_011534534.1:n.346+67_346+68insC
XM_017011436.2:c.346+67_346+68insC (CCNC)	XP_016866925.1:n.346+67_346+68insC
XR_001743062.2:n.661-20033_661-20032insG (TSTD3)
XR_001743714.2:n.463+67_463+68insC (CCNC)
NM_005190.4:c.346+67_346+68insC (CCNC) MANE Select	NP_005181.2:n.346+67_346+68insC
NM_001013399.2:c.91+67_91+68insC (CCNC)	NP_001013417.1:n.91+67_91+68insC
NM_001363537.2:c.346+67_346+68insC (CCNC)	NP_001350466.1:n.346+67_346+68insC