Canonical Allele Identifier: CA1655198576
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112060972C= , CM000668.2:g.112060972C= GRCh38
NC_000006.11:g.112382175C= , CM000668.1:g.112382175C= GRCh37
NC_000006.10:g.112488868C= NCBI36
NG_011748.1:g.11898C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.49-19C= MANE Select ENSP00000357655.4:n.49-19C=
ENST00000230529.9:c.49-19C= ENSP00000230529.5:n.49-19C=
ENST00000361714.5:c.49-19C= ENSP00000354734.2:n.49-19C=
ENST00000368663.4:c.49-19C= ENSP00000357652.4:n.49-19C=
ENST00000368664.7:c.103-19C= ENSP00000357653.3:n.103-19C=
ENST00000368666.6:c.103-19C= ENSP00000357655.3:n.103-19C=
ENST00000409166.5:c.-507-307C= ENSP00000386467.1:n.-507-307C=
ENST00000454589.5:c.49-19C= ENSP00000395928.1:n.49-19C=
ENST00000604763.5:c.49-19C= ENSP00000473777.1:n.49-19C=
ENST00000620524.3:n.64-100C=
NM_003880.3:c.49-19C= NP_003871.1:n.49-19C=
NM_198239.1:c.103-19C= NP_937882.1:n.103-19C=
NR_125353.1:n.239-19C=
NR_125354.1:n.159-19C=
XM_011536220.1:c.49-19C= XP_011534522.1:n.49-19C=
XM_011536221.1:c.112-19C= XP_011534523.1:n.112-19C=
XM_011536222.1:c.187-19C= XP_011534524.1:n.187-19C=
XM_011536222.2:c.112-19C= XP_011534524.2:n.112-19C=
XR_001743705.1:n.587-19C=
NM_003880.4:c.49-19C= NP_003871.1:n.49-19C=
NM_198239.2:c.49-19C= MANE Select NP_937882.2:n.49-19C=
NR_125353.2:n.303-19C=
NR_125354.3:n.130-19C=