Canonical Allele Identifier: CA365376110

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390648G>T (hg19) ; chr6:g.112069445G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069445G>T , CM000668.2:g.112069445G>T	GRCh38
NC_000006.11:g.112390648G>T , CM000668.1:g.112390648G>T	GRCh37
NC_000006.10:g.112497341G>T	NCBI36
NG_011748.1:g.20371G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.890G>T MANE Select	ENSP00000357655.4:p.Gly297Val
ENST00000639360.1:c.791G>T	ENSP00000491774.1:p.Gly264Val
ENST00000230529.9:c.890G>T	ENSP00000230529.5:p.Gly297Val
ENST00000361714.5:c.890G>T	ENSP00000354734.2:p.Gly297Val
ENST00000368663.4:c.*196G>T	ENSP00000357652.4:n.*196G>T
ENST00000368664.7:c.*294G>T	ENSP00000357653.3:n.*294G>T
ENST00000368666.6:c.944G>T	ENSP00000357655.3:p.Gly315Val
ENST00000409166.5:c.218G>T	ENSP00000386467.1:p.Gly73Val
ENST00000454589.5:c.*294G>T	ENSP00000395928.1:n.*294G>T
ENST00000604763.5:c.890G>T	ENSP00000473777.1:p.Gly297Val
ENST00000613648.1:n.725G>T
ENST00000620524.3:n.821G>T
NM_003880.3:c.890G>T	NP_003871.1:p.Gly297Val
NM_198239.1:c.944G>T	NP_937882.1:p.Gly315Val
NR_125353.1:n.1144G>T
NR_125354.1:n.1064G>T
XM_011536220.1:c.890G>T	XP_011534522.1:p.Gly297Val
XM_011536221.1:c.*294G>T	XP_011534523.1:n.*294G>T
XM_011536223.1:c.308G>T	XP_011534525.1:p.Gly103Val
XM_011536223.3:c.308G>T	XP_011534525.1:p.Gly103Val
XR_001743705.1:n.1492G>T
NM_003880.4:c.890G>T	NP_003871.1:p.Gly297Val
NM_198239.2:c.890G>T MANE Select	NP_937882.2:p.Gly297Val
NR_125353.2:n.1208G>T
NR_125354.3:n.1035G>T