Canonical Allele Identifier: CA365376706

Gene: CCN6

Linked Data

• dbSNP Id: rs782086415
• MyVariant Identifiers: chr6:g.112390759C>T (hg19) ; chr6:g.112069556C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069556C>T , CM000668.2:g.112069556C>T	GRCh38
NC_000006.11:g.112390759C>T , CM000668.1:g.112390759C>T	GRCh37
NC_000006.10:g.112497452C>T	NCBI36
NG_011748.1:g.20482C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1001C>T MANE Select	ENSP00000357655.4:p.Ser334Phe
ENST00000639360.1:c.902C>T	ENSP00000491774.1:p.Ser301Phe
ENST00000230529.9:c.1001C>T	ENSP00000230529.5:p.Ser334Phe
ENST00000361714.5:c.1001C>T	ENSP00000354734.2:p.Ser334Phe
ENST00000368663.4:c.*307C>T	ENSP00000357652.4:n.*307C>T
ENST00000368664.7:c.*405C>T	ENSP00000357653.3:n.*405C>T
ENST00000368666.6:c.1055C>T	ENSP00000357655.3:p.Ser352Phe
ENST00000409166.5:c.329C>T	ENSP00000386467.1:p.Ser110Phe
ENST00000454589.5:c.*405C>T	ENSP00000395928.1:n.*405C>T
ENST00000604763.5:c.1001C>T	ENSP00000473777.1:p.Ser334Phe
ENST00000613648.1:n.836C>T
ENST00000620524.3:n.932C>T
NM_003880.3:c.1001C>T	NP_003871.1:p.Ser334Phe
NM_198239.1:c.1055C>T	NP_937882.1:p.Ser352Phe
NR_125353.1:n.1255C>T
NR_125354.1:n.1175C>T
XM_011536220.1:c.1001C>T	XP_011534522.1:p.Ser334Phe
XM_011536221.1:c.*405C>T	XP_011534523.1:n.*405C>T
XM_011536223.1:c.419C>T	XP_011534525.1:p.Ser140Phe
XM_011536223.3:c.419C>T	XP_011534525.1:p.Ser140Phe
XR_001743705.1:n.1603C>T
NM_003880.4:c.1001C>T	NP_003871.1:p.Ser334Phe
NM_198239.2:c.1001C>T MANE Select	NP_937882.2:p.Ser334Phe
NR_125353.2:n.1319C>T
NR_125354.3:n.1146C>T