Canonical Allele Identifier: CA1655198634
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112061094C= , CM000668.2:g.112061094C= GRCh38
NC_000006.11:g.112382297C= , CM000668.1:g.112382297C= GRCh37
NC_000006.10:g.112488990C= NCBI36
NG_011748.1:g.12020C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368666.7:c.152C= MANE Select ENSP00000357655.4:p.Pro51=
ENST00000639360.1:c.56C= ENSP00000491774.1:p.Pro19=
ENST00000230529.9:c.152C= ENSP00000230529.5:p.Pro51=
ENST00000361714.5:c.152C= ENSP00000354734.2:p.Pro51=
ENST00000368663.4:c.152C= ENSP00000357652.4:p.Pro51=
ENST00000368664.7:c.206C= ENSP00000357653.3:p.Pro69=
ENST00000368666.6:c.206C= ENSP00000357655.3:p.Pro69=
ENST00000409166.5:c.-507-185C= ENSP00000386467.1:n.-507-185C=
ENST00000454589.5:c.152C= ENSP00000395928.1:p.Pro51=
ENST00000604763.5:c.152C= ENSP00000473777.1:p.Pro51=
ENST00000620524.3:n.86C=
NM_003880.3:c.152C= NP_003871.1:p.Pro51=
NM_198239.1:c.206C= NP_937882.1:p.Pro69=
NR_125353.1:n.342C=
NR_125354.1:n.262C=
XM_011536220.1:c.152C= XP_011534522.1:p.Pro51=
XM_011536221.1:c.215C= XP_011534523.1:p.Pro72=
XM_011536222.1:c.290C= XP_011534524.1:p.Pro97=
XM_011536222.2:c.215C= XP_011534524.2:p.Pro72=
XR_001743705.1:n.690C=
NM_003880.4:c.152C= NP_003871.1:p.Pro51=
NM_198239.2:c.152C= MANE Select NP_937882.2:p.Pro51=
NR_125353.2:n.406C=
NR_125354.3:n.233C=