Canonical Allele Identifier: CA451901430

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069554-A-C
• MyVariant Identifiers: chr6:g.112390757A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069554A>C , CM000668.2:g.112069554A>C	GRCh38
NC_000006.11:g.112390757A>C , CM000668.1:g.112390757A>C	GRCh37
NC_000006.10:g.112497450A>C	NCBI36
NG_011748.1:g.20480A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.999A>C MANE Select	ENSP00000357655.4:p.Thr333=
ENST00000639360.1:c.900A>C	ENSP00000491774.1:p.Thr300=
ENST00000230529.9:c.999A>C	ENSP00000230529.5:p.Thr333=
ENST00000361714.5:c.999A>C	ENSP00000354734.2:p.Thr333=
ENST00000368663.4:c.*305A>C	ENSP00000357652.4:n.*305A>C
ENST00000368664.7:c.*403A>C	ENSP00000357653.3:n.*403A>C
ENST00000368666.6:c.1053A>C	ENSP00000357655.3:p.Thr351=
ENST00000409166.5:c.327A>C	ENSP00000386467.1:p.Thr109=
ENST00000454589.5:c.*403A>C	ENSP00000395928.1:n.*403A>C
ENST00000604763.5:c.999A>C	ENSP00000473777.1:p.Thr333=
ENST00000613648.1:n.834A>C
ENST00000620524.3:n.930A>C
NM_003880.3:c.999A>C	NP_003871.1:p.Thr333=
NM_198239.1:c.1053A>C	NP_937882.1:p.Thr351=
NR_125353.1:n.1253A>C
NR_125354.1:n.1173A>C
XM_011536220.1:c.999A>C	XP_011534522.1:p.Thr333=
XM_011536221.1:c.*403A>C	XP_011534523.1:n.*403A>C
XM_011536223.1:c.417A>C	XP_011534525.1:p.Thr139=
XM_011536223.3:c.417A>C	XP_011534525.1:p.Thr139=
XR_001743705.1:n.1601A>C
NM_003880.4:c.999A>C	NP_003871.1:p.Thr333=
NM_198239.2:c.999A>C MANE Select	NP_937882.2:p.Thr333=
NR_125353.2:n.1317A>C
NR_125354.3:n.1144A>C