Canonical Allele Identifier: CA365377077

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069610-A-C
• MyVariant Identifiers: chr6:g.112390813A>C (hg19) ; chr6:g.112069610A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069610A>C , CM000668.2:g.112069610A>C	GRCh38
NC_000006.11:g.112390813A>C , CM000668.1:g.112390813A>C	GRCh37
NC_000006.10:g.112497506A>C	NCBI36
NG_011748.1:g.20536A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1055A>C MANE Select	ENSP00000357655.4:p.Lys352Thr
ENST00000639360.1:c.956A>C	ENSP00000491774.1:p.Lys319Thr
ENST00000230529.9:c.1055A>C	ENSP00000230529.5:p.Lys352Thr
ENST00000361714.5:c.1055A>C	ENSP00000354734.2:p.Lys352Thr
ENST00000368663.4:c.*361A>C	ENSP00000357652.4:n.*361A>C
ENST00000368664.7:c.*459A>C	ENSP00000357653.3:n.*459A>C
ENST00000368666.6:c.1109A>C	ENSP00000357655.3:p.Lys370Thr
ENST00000409166.5:c.383A>C	ENSP00000386467.1:p.Lys128Thr
ENST00000454589.5:c.*459A>C	ENSP00000395928.1:n.*459A>C
ENST00000604763.5:c.1055A>C	ENSP00000473777.1:p.Lys352Thr
ENST00000613648.1:n.890A>C
ENST00000620524.3:n.986A>C
NM_003880.3:c.1055A>C	NP_003871.1:p.Lys352Thr
NM_198239.1:c.1109A>C	NP_937882.1:p.Lys370Thr
NR_125353.1:n.1309A>C
NR_125354.1:n.1229A>C
XM_011536220.1:c.1055A>C	XP_011534522.1:p.Lys352Thr
XM_011536221.1:c.*459A>C	XP_011534523.1:n.*459A>C
XM_011536223.1:c.473A>C	XP_011534525.1:p.Lys158Thr
XM_011536223.3:c.473A>C	XP_011534525.1:p.Lys158Thr
XR_001743705.1:n.1657A>C
NM_003880.4:c.1055A>C	NP_003871.1:p.Lys352Thr
NM_198239.2:c.1055A>C MANE Select	NP_937882.2:p.Lys352Thr
NR_125353.2:n.1373A>C
NR_125354.3:n.1200A>C