Canonical Allele Identifier: CA4886100

Gene: CCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133213085G>A , CM000670.2:g.133213085G>A	GRCh38
NC_000008.10:g.134225328G>A , CM000670.1:g.134225328G>A	GRCh37
NC_000008.9:g.134294510G>A	NCBI36
NG_029529.1:g.27047G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003882.4:c.291G>A MANE Select	NP_003873.1:p.Arg97=
ENST00000250160.11:c.291G>A MANE Select	ENSP00000250160.5:p.Arg97=
NM_001204869.1:c.291G>A	NP_001191798.1:p.Arg97=
NM_001204869.2:c.291G>A	NP_001191798.1:p.Arg97=
NM_001204870.1:c.70-14326G>A	NP_001191799.1:n.70-14326G>A
NM_001204870.2:c.70-14326G>A	NP_001191799.1:n.70-14326G>A
NM_003882.3:c.291G>A	NP_003873.1:p.Arg97=
NM_080838.2:c.291G>A	NP_543028.1:p.Arg97=
NM_080838.3:c.291G>A	NP_543028.1:p.Arg97=
NR_037944.1:n.176-12305G>A
NR_037944.2:n.176-12305G>A
ENST00000220856.6:c.291G>A	ENSP00000220856.6:p.Arg97=
ENST00000250160.10:c.291G>A	ENSP00000250160.5:p.Arg97=
ENST00000377862.6:c.70-12305G>A	ENSP00000367093.2:n.70-12305G>A
ENST00000517423.5:c.291G>A	ENSP00000427744.1:p.Arg97=
ENST00000519433.1:c.70-14326G>A	ENSP00000429185.1:n.70-14326G>A
XM_006716680.2:c.80G>A	XP_006716743.1:p.Gly27Glu
XM_011517358.1:c.80G>A	XP_011515660.1:p.Gly27Glu
XM_024447319.1:c.80G>A	XP_024303087.1:p.Gly27Glu
XM_024447320.1:c.80G>A	XP_024303088.1:p.Gly27Glu