Canonical Allele Identifier: CA1655198577
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112060975T= , CM000668.2:g.112060975T= GRCh38
NC_000006.11:g.112382178T= , CM000668.1:g.112382178T= GRCh37
NC_000006.10:g.112488871T= NCBI36
NG_011748.1:g.11901T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.49-16T= MANE Select ENSP00000357655.4:n.49-16T=
ENST00000230529.9:c.49-16T= ENSP00000230529.5:n.49-16T=
ENST00000361714.5:c.49-16T= ENSP00000354734.2:n.49-16T=
ENST00000368663.4:c.49-16T= ENSP00000357652.4:n.49-16T=
ENST00000368664.7:c.103-16T= ENSP00000357653.3:n.103-16T=
ENST00000368666.6:c.103-16T= ENSP00000357655.3:n.103-16T=
ENST00000409166.5:c.-507-304T= ENSP00000386467.1:n.-507-304T=
ENST00000454589.5:c.49-16T= ENSP00000395928.1:n.49-16T=
ENST00000604763.5:c.49-16T= ENSP00000473777.1:n.49-16T=
ENST00000620524.3:n.64-97T=
NM_003880.3:c.49-16T= NP_003871.1:n.49-16T=
NM_198239.1:c.103-16T= NP_937882.1:n.103-16T=
NR_125353.1:n.239-16T=
NR_125354.1:n.159-16T=
XM_011536220.1:c.49-16T= XP_011534522.1:n.49-16T=
XM_011536221.1:c.112-16T= XP_011534523.1:n.112-16T=
XM_011536222.1:c.187-16T= XP_011534524.1:n.187-16T=
XM_011536222.2:c.112-16T= XP_011534524.2:n.112-16T=
XR_001743705.1:n.587-16T=
NM_003880.4:c.49-16T= NP_003871.1:n.49-16T=
NM_198239.2:c.49-16T= MANE Select NP_937882.2:n.49-16T=
NR_125353.2:n.303-16T=
NR_125354.3:n.130-16T=