Canonical Allele Identifier: CA451901180

Gene: CCN6

Linked Data

• gnomAD v4: 6-112061182-G-A
• MyVariant Identifiers: chr6:g.112382385G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061182G>A , CM000668.2:g.112061182G>A	GRCh38
NC_000006.11:g.112382385G>A , CM000668.1:g.112382385G>A	GRCh37
NC_000006.10:g.112489078G>A	NCBI36
NG_011748.1:g.12108G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.240G>A MANE Select	ENSP00000357655.4:p.Lys80=
ENST00000639360.1:c.144G>A	ENSP00000491774.1:p.Lys48=
ENST00000230529.9:c.240G>A	ENSP00000230529.5:p.Lys80=
ENST00000361714.5:c.240G>A	ENSP00000354734.2:p.Lys80=
ENST00000368663.4:c.240G>A	ENSP00000357652.4:p.Lys80=
ENST00000368664.7:c.294G>A	ENSP00000357653.3:p.Lys98=
ENST00000368666.6:c.294G>A	ENSP00000357655.3:p.Lys98=
ENST00000409166.5:c.-507-97G>A	ENSP00000386467.1:n.-507-97G>A
ENST00000454589.5:c.240G>A	ENSP00000395928.1:p.Lys80=
ENST00000604763.5:c.240G>A	ENSP00000473777.1:p.Lys80=
ENST00000620524.3:n.174G>A
NM_003880.3:c.240G>A	NP_003871.1:p.Lys80=
NM_198239.1:c.294G>A	NP_937882.1:p.Lys98=
NR_125353.1:n.430G>A
NR_125354.1:n.350G>A
XM_011536220.1:c.240G>A	XP_011534522.1:p.Lys80=
XM_011536221.1:c.303G>A	XP_011534523.1:p.Lys101=
XM_011536222.1:c.378G>A	XP_011534524.1:p.Lys126=
XM_011536222.2:c.303G>A	XP_011534524.2:p.Lys101=
XR_001743705.1:n.778G>A
NM_003880.4:c.240G>A	NP_003871.1:p.Lys80=
NM_198239.2:c.240G>A MANE Select	NP_937882.2:p.Lys80=
NR_125353.2:n.494G>A
NR_125354.3:n.321G>A