Canonical Allele Identifier: CA2680045430

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069675-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069675G>T , CM000668.2:g.112069675G>T	GRCh38
NC_000006.11:g.112390878G>T , CM000668.1:g.112390878G>T	GRCh37
NC_000006.10:g.112497571G>T	NCBI36
NG_011748.1:g.20601G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*55G>T MANE Select	ENSP00000357655.4:n.*55G>T
ENST00000639360.1:c.1021G>T	ENSP00000491774.1:n.1021G>T
ENST00000230529.9:c.*55G>T	ENSP00000230529.5:n.*55G>T
ENST00000361714.5:c.*55G>T	ENSP00000354734.2:n.*55G>T
ENST00000368666.6:c.*55G>T	ENSP00000357655.3:n.*55G>T
ENST00000454589.5:c.*524G>T	ENSP00000395928.1:n.*524G>T
ENST00000604763.5:c.*55G>T	ENSP00000473777.1:n.*55G>T
ENST00000620524.3:n.1051G>T
NM_003880.3:c.*55G>T	NP_003871.1:n.*55G>T
NM_198239.1:c.*55G>T	NP_937882.1:n.*55G>T
NR_125353.1:n.1374G>T
NR_125354.1:n.1294G>T
XM_011536220.1:c.*55G>T	XP_011534522.1:n.*55G>T
XM_011536221.1:c.*524G>T	XP_011534523.1:n.*524G>T
XM_011536223.1:c.*55G>T	XP_011534525.1:n.*55G>T
XM_011536223.3:c.*55G>T	XP_011534525.1:n.*55G>T
XR_001743705.1:n.1722G>T
NM_003880.4:c.*55G>T	NP_003871.1:n.*55G>T
NM_198239.2:c.*55G>T MANE Select	NP_937882.2:n.*55G>T
NR_125353.2:n.1438G>T
NR_125354.3:n.1265G>T