Canonical Allele Identifier: CA1821150546

Gene: CCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133207820G= , CM000670.2:g.133207820G=	GRCh38
NC_000008.10:g.134220063G= , CM000670.1:g.134220063G=	GRCh37
NC_000008.9:g.134289245G=	NCBI36
NG_029529.1:g.21782G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003882.4:c.70-5044G= MANE Select	NP_003873.1:n.70-5044G=
ENST00000250160.11:c.70-5044G= MANE Select	ENSP00000250160.5:n.70-5044G=
NM_001204869.1:c.70-5044G=	NP_001191798.1:n.70-5044G=
NM_001204869.2:c.70-5044G=	NP_001191798.1:n.70-5044G=
NM_001204870.1:c.69+16607G=	NP_001191799.1:n.69+16607G=
NM_001204870.2:c.69+16607G=	NP_001191799.1:n.69+16607G=
NM_003882.3:c.70-5044G=	NP_003873.1:n.70-5044G=
NM_080838.2:c.70-5044G=	NP_543028.1:n.70-5044G=
NM_080838.3:c.70-5044G=	NP_543028.1:n.70-5044G=
NR_037944.1:n.175+16607G=
NR_037944.2:n.175+16607G=
ENST00000220856.6:c.70-5044G=	ENSP00000220856.6:n.70-5044G=
ENST00000250160.10:c.70-5044G=	ENSP00000250160.5:n.70-5044G=
ENST00000377862.6:c.69+16607G=	ENSP00000367093.2:n.69+16607G=
ENST00000517423.5:c.70-5044G=	ENSP00000427744.1:n.70-5044G=
ENST00000519433.1:c.69+16607G=	ENSP00000429185.1:n.69+16607G=
XM_024447319.1:c.-142-5044G=	XP_024303087.1:n.-142-5044G=
XM_024447320.1:c.-142-5044G=	XP_024303088.1:n.-142-5044G=