Canonical Allele Identifier: CA365368541
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112061070A>T , CM000668.2:g.112061070A>T GRCh38
NC_000006.11:g.112382273A>T , CM000668.1:g.112382273A>T GRCh37
NC_000006.10:g.112488966A>T NCBI36
NG_011748.1:g.11996A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.128A>T MANE Select ENSP00000357655.4:p.Gln43Leu
ENST00000639360.1:c.32A>T ENSP00000491774.1:p.Gln11Leu
ENST00000230529.9:c.128A>T ENSP00000230529.5:p.Gln43Leu
ENST00000361714.5:c.128A>T ENSP00000354734.2:p.Gln43Leu
ENST00000368663.4:c.128A>T ENSP00000357652.4:p.Gln43Leu
ENST00000368664.7:c.182A>T ENSP00000357653.3:p.Gln61Leu
ENST00000368666.6:c.182A>T ENSP00000357655.3:p.Gln61Leu
ENST00000409166.5:c.-507-209A>T ENSP00000386467.1:n.-507-209A>T
ENST00000454589.5:c.128A>T ENSP00000395928.1:p.Gln43Leu
ENST00000604763.5:c.128A>T ENSP00000473777.1:p.Gln43Leu
ENST00000620524.3:n.64-2A>T
NM_003880.3:c.128A>T NP_003871.1:p.Gln43Leu
NM_198239.1:c.182A>T NP_937882.1:p.Gln61Leu
NR_125353.1:n.318A>T
NR_125354.1:n.238A>T
XM_011536220.1:c.128A>T XP_011534522.1:p.Gln43Leu
XM_011536221.1:c.191A>T XP_011534523.1:p.Gln64Leu
XM_011536222.1:c.266A>T XP_011534524.1:p.Gln89Leu
XM_011536222.2:c.191A>T XP_011534524.2:p.Gln64Leu
XR_001743705.1:n.666A>T
NM_003880.4:c.128A>T NP_003871.1:p.Gln43Leu
NM_198239.2:c.128A>T MANE Select NP_937882.2:p.Gln43Leu
NR_125353.2:n.382A>T
NR_125354.3:n.209A>T