Canonical Allele Identifier: CA451900777

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382196C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112060993C>T , CM000668.2:g.112060993C>T	GRCh38
NC_000006.11:g.112382196C>T , CM000668.1:g.112382196C>T	GRCh37
NC_000006.10:g.112488889C>T	NCBI36
NG_011748.1:g.11919C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.51C>T MANE Select	ENSP00000357655.4:p.Phe17=
ENST00000230529.9:c.51C>T	ENSP00000230529.5:p.Phe17=
ENST00000361714.5:c.51C>T	ENSP00000354734.2:p.Phe17=
ENST00000368663.4:c.51C>T	ENSP00000357652.4:p.Phe17=
ENST00000368664.7:c.105C>T	ENSP00000357653.3:p.Phe35=
ENST00000368666.6:c.105C>T	ENSP00000357655.3:p.Phe35=
ENST00000409166.5:c.-507-286C>T	ENSP00000386467.1:n.-507-286C>T
ENST00000454589.5:c.51C>T	ENSP00000395928.1:p.Phe17=
ENST00000604763.5:c.51C>T	ENSP00000473777.1:p.Phe17=
ENST00000620524.3:n.64-79C>T
NM_003880.3:c.51C>T	NP_003871.1:p.Phe17=
NM_198239.1:c.105C>T	NP_937882.1:p.Phe35=
NR_125353.1:n.241C>T
NR_125354.1:n.161C>T
XM_011536220.1:c.51C>T	XP_011534522.1:p.Phe17=
XM_011536221.1:c.114C>T	XP_011534523.1:p.Phe38=
XM_011536222.1:c.189C>T	XP_011534524.1:p.Phe63=
XM_011536222.2:c.114C>T	XP_011534524.2:p.Phe38=
XR_001743705.1:n.589C>T
NM_003880.4:c.51C>T	NP_003871.1:p.Phe17=
NM_198239.2:c.51C>T MANE Select	NP_937882.2:p.Phe17=
NR_125353.2:n.305C>T
NR_125354.3:n.132C>T