Canonical Allele Identifier: CA1821155392

Gene: CCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133230265G= , CM000670.2:g.133230265G=	GRCh38
NC_000008.10:g.134242508G= , CM000670.1:g.134242508G=	GRCh37
NC_000008.9:g.134311690G=	NCBI36
NG_029529.1:g.44227G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250160.11:c.*2555G= MANE Select	ENSP00000250160.5:n.*2555G=
ENST00000250160.10:c.*2555G=	ENSP00000250160.5:n.*2555G=
NM_001204869.1:c.*2736G=	NP_001191798.1:n.*2736G=
NM_001204870.1:c.*2555G=	NP_001191799.1:n.*2555G=
NM_003882.3:c.*2555G=	NP_003873.1:n.*2555G=
NM_080838.2:c.*2555G=	NP_543028.1:n.*2555G=
NR_037944.1:n.3224G=
XM_006716680.2:c.*2555G=	XP_006716743.1:n.*2555G=
XM_011517358.1:c.*2555G=	XP_011515660.1:n.*2555G=
XM_011517359.1:c.*2555G=	XP_011515661.1:n.*2555G=
XM_024447319.1:c.*2555G=	XP_024303087.1:n.*2555G=
XM_024447320.1:c.*2555G=	XP_024303088.1:n.*2555G=
XM_024447321.1:c.*2555G=	XP_024303089.1:n.*2555G=
NM_003882.4:c.*2555G= MANE Select	NP_003873.1:n.*2555G=
NM_001204869.2:c.*2736G=	NP_001191798.1:n.*2736G=
NM_001204870.2:c.*2555G=	NP_001191799.1:n.*2555G=
NM_080838.3:c.*2555G=	NP_543028.1:n.*2555G=
NR_037944.2:n.3224G=