Canonical Allele Identifier: CA365369407

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382380G>T (hg19) ; chr6:g.112061177G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061177G>T , CM000668.2:g.112061177G>T	GRCh38
NC_000006.11:g.112382380G>T , CM000668.1:g.112382380G>T	GRCh37
NC_000006.10:g.112489073G>T	NCBI36
NG_011748.1:g.12103G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.235G>T MANE Select	ENSP00000357655.4:p.Ala79Ser
ENST00000639360.1:c.139G>T	ENSP00000491774.1:p.Ala47Ser
ENST00000230529.9:c.235G>T	ENSP00000230529.5:p.Ala79Ser
ENST00000361714.5:c.235G>T	ENSP00000354734.2:p.Ala79Ser
ENST00000368663.4:c.235G>T	ENSP00000357652.4:p.Ala79Ser
ENST00000368664.7:c.289G>T	ENSP00000357653.3:p.Ala97Ser
ENST00000368666.6:c.289G>T	ENSP00000357655.3:p.Ala97Ser
ENST00000409166.5:c.-507-102G>T	ENSP00000386467.1:n.-507-102G>T
ENST00000454589.5:c.235G>T	ENSP00000395928.1:p.Ala79Ser
ENST00000604763.5:c.235G>T	ENSP00000473777.1:p.Ala79Ser
ENST00000620524.3:n.169G>T
NM_003880.3:c.235G>T	NP_003871.1:p.Ala79Ser
NM_198239.1:c.289G>T	NP_937882.1:p.Ala97Ser
NR_125353.1:n.425G>T
NR_125354.1:n.345G>T
XM_011536220.1:c.235G>T	XP_011534522.1:p.Ala79Ser
XM_011536221.1:c.298G>T	XP_011534523.1:p.Ala100Ser
XM_011536222.1:c.373G>T	XP_011534524.1:p.Ala125Ser
XM_011536222.2:c.298G>T	XP_011534524.2:p.Ala100Ser
XR_001743705.1:n.773G>T
NM_003880.4:c.235G>T	NP_003871.1:p.Ala79Ser
NM_198239.2:c.235G>T MANE Select	NP_937882.2:p.Ala79Ser
NR_125353.2:n.489G>T
NR_125354.3:n.316G>T