Canonical Allele Identifier: CA12900604

Gene: CCN4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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