Canonical Allele Identifier: CA1821155393

Gene: CCN4

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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