Canonical Allele Identifier: CA4886103

Gene: CCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133213091C>T , CM000670.2:g.133213091C>T	GRCh38
NC_000008.10:g.134225334C>T , CM000670.1:g.134225334C>T	GRCh37
NC_000008.9:g.134294516C>T	NCBI36
NG_029529.1:g.27053C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250160.11:c.297C>T MANE Select	ENSP00000250160.5:p.Leu99=
ENST00000220856.6:c.297C>T	ENSP00000220856.6:p.Leu99=
ENST00000250160.10:c.297C>T	ENSP00000250160.5:p.Leu99=
ENST00000377862.6:c.70-12299C>T	ENSP00000367093.2:n.70-12299C>T
ENST00000517423.5:c.297C>T	ENSP00000427744.1:p.Leu99=
ENST00000519433.1:c.70-14320C>T	ENSP00000429185.1:n.70-14320C>T
NM_001204869.1:c.297C>T	NP_001191798.1:p.Leu99=
NM_001204870.1:c.70-14320C>T	NP_001191799.1:n.70-14320C>T
NM_003882.3:c.297C>T	NP_003873.1:p.Leu99=
NM_080838.2:c.297C>T	NP_543028.1:p.Leu99=
NR_037944.1:n.176-12299C>T
XM_006716680.2:c.86C>T	XP_006716743.1:p.Ser29Phe
XM_011517358.1:c.86C>T	XP_011515660.1:p.Ser29Phe
XM_024447319.1:c.86C>T	XP_024303087.1:p.Ser29Phe
XM_024447320.1:c.86C>T	XP_024303088.1:p.Ser29Phe
NM_003882.4:c.297C>T MANE Select	NP_003873.1:p.Leu99=
NM_001204869.2:c.297C>T	NP_001191798.1:p.Leu99=
NM_001204870.2:c.70-14320C>T	NP_001191799.1:n.70-14320C>T
NM_080838.3:c.297C>T	NP_543028.1:p.Leu99=
NR_037944.2:n.176-12299C>T