Canonical Allele Identifier: CA1139900810

Gene: CCDC190

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162851501A= , CM000663.2:g.162851501A=	GRCh38
NC_000001.10:g.162821291A= , CM000663.1:g.162821291A=	GRCh37
NC_000001.9:g.161087915A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367912.7:c.*3264T= MANE Select	ENSP00000356888.3:n.*3264T=
ENST00000367912.6:c.*1621T=	ENSP00000356888.2:n.*1621T=
ENST00000524691.1:n.152+4131T=
XM_005245125.2:c.*3264T=	XP_005245182.1:n.*3264T=
XM_006711289.2:c.*3264T=	XP_006711352.1:n.*3264T=
XM_011509477.1:c.*3264T=	XP_011507779.1:n.*3264T=
XR_921772.1:n.4749+15T=
XM_005245125.3:c.*3264T=	XP_005245182.1:n.*3264T=
XM_006711289.3:c.*3264T=	XP_006711352.1:n.*3264T=
XM_011509477.2:c.*3264T=	XP_011507779.1:n.*3264T=
NM_001394065.1:c.*3264T= MANE Select	NP_001380994.1:n.*3264T=
NM_178550.6:c.*3264T=	NP_848645.3:n.*3264T=