Canonical Allele Identifier: CA2695206859

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061178_112061179delinsAA , CM000668.2:g.112061178_112061179delinsAA	GRCh38
NC_000006.11:g.112382381_112382382delinsAA , CM000668.1:g.112382381_112382382delinsAA	GRCh37
NC_000006.10:g.112489074_112489075delinsAA	NCBI36
NG_011748.1:g.12104_12105delinsAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.236_237delinsAA MANE Select	ENSP00000357655.4:p.Ala79Glu
ENST00000639360.1:c.140_141delinsAA	ENSP00000491774.1:p.Ala47Glu
ENST00000230529.9:c.236_237delinsAA	ENSP00000230529.5:p.Ala79Glu
ENST00000361714.5:c.236_237delinsAA	ENSP00000354734.2:p.Ala79Glu
ENST00000368663.4:c.236_237delinsAA	ENSP00000357652.4:p.Ala79Glu
ENST00000368664.7:c.290_291delinsAA	ENSP00000357653.3:p.Ala97Glu
ENST00000368666.6:c.290_291delinsAA	ENSP00000357655.3:p.Ala97Glu
ENST00000409166.5:c.-507-101_-507-100delinsAA	ENSP00000386467.1:n.-507-101_-507-100deli...
ENST00000454589.5:c.236_237delinsAA	ENSP00000395928.1:p.Ala79Glu
ENST00000604763.5:c.236_237delinsAA	ENSP00000473777.1:p.Ala79Glu
ENST00000620524.3:n.170_171delinsAA
NM_003880.3:c.236_237delinsAA	NP_003871.1:p.Ala79Glu
NM_198239.1:c.290_291delinsAA	NP_937882.1:p.Ala97Glu
NR_125353.1:n.426_427delinsAA
NR_125354.1:n.346_347delinsAA
XM_011536220.1:c.236_237delinsAA	XP_011534522.1:p.Ala79Glu
XM_011536221.1:c.299_300delinsAA	XP_011534523.1:p.Ala100Glu
XM_011536222.1:c.374_375delinsAA	XP_011534524.1:p.Ala125Glu
XM_011536222.2:c.299_300delinsAA	XP_011534524.2:p.Ala100Glu
XR_001743705.1:n.774_775delinsAA
NM_003880.4:c.236_237delinsAA	NP_003871.1:p.Ala79Glu
NM_198239.2:c.236_237delinsAA MANE Select	NP_937882.2:p.Ala79Glu
NR_125353.2:n.490_491delinsAA
NR_125354.3:n.317_318delinsAA