Canonical Allele Identifier: CA365376796

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390770C>T (hg19) ; chr6:g.112069567C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069567C>T , CM000668.2:g.112069567C>T	GRCh38
NC_000006.11:g.112390770C>T , CM000668.1:g.112390770C>T	GRCh37
NC_000006.10:g.112497463C>T	NCBI36
NG_011748.1:g.20493C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1012C>T MANE Select	ENSP00000357655.4:p.Gln338Ter
ENST00000639360.1:c.913C>T	ENSP00000491774.1:p.Gln305Ter
ENST00000230529.9:c.1012C>T	ENSP00000230529.5:p.Gln338Ter
ENST00000361714.5:c.1012C>T	ENSP00000354734.2:p.Gln338Ter
ENST00000368663.4:c.*318C>T	ENSP00000357652.4:n.*318C>T
ENST00000368664.7:c.*416C>T	ENSP00000357653.3:n.*416C>T
ENST00000368666.6:c.1066C>T	ENSP00000357655.3:p.Gln356Ter
ENST00000409166.5:c.340C>T	ENSP00000386467.1:p.Gln114Ter
ENST00000454589.5:c.*416C>T	ENSP00000395928.1:n.*416C>T
ENST00000604763.5:c.1012C>T	ENSP00000473777.1:p.Gln338Ter
ENST00000613648.1:n.847C>T
ENST00000620524.3:n.943C>T
NM_003880.3:c.1012C>T	NP_003871.1:p.Gln338Ter
NM_198239.1:c.1066C>T	NP_937882.1:p.Gln356Ter
NR_125353.1:n.1266C>T
NR_125354.1:n.1186C>T
XM_011536220.1:c.1012C>T	XP_011534522.1:p.Gln338Ter
XM_011536221.1:c.*416C>T	XP_011534523.1:n.*416C>T
XM_011536223.1:c.430C>T	XP_011534525.1:p.Gln144Ter
XM_011536223.3:c.430C>T	XP_011534525.1:p.Gln144Ter
XR_001743705.1:n.1614C>T
NM_003880.4:c.1012C>T	NP_003871.1:p.Gln338Ter
NM_198239.2:c.1012C>T MANE Select	NP_937882.2:p.Gln338Ter
NR_125353.2:n.1330C>T
NR_125354.3:n.1157C>T