Canonical Allele Identifier: CA1332796155

Gene: COL4A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227164969C= , CM000664.2:g.227164969C=	GRCh38
NC_000002.11:g.228029685C= , CM000664.1:g.228029685C=	GRCh37
NC_000002.10:g.227737929C=	NCBI36
NG_011591.1:g.5405C= , LRG_230:g.5405C=
NG_011592.1:g.4591G= , LRG_231:g.4591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396578.8:c.87+156C= MANE Select	ENSP00000379823.3:n.87+156C=
ENST00000396578.7:c.87+156C=	ENSP00000379823.3:n.87+156C=
NM_000091.4:c.87+156C= , LRG_230t1:c.87+156C=	NP_000082.2:n.87+156C=
XM_005246276.2:c.87+156C=	XP_005246333.1:n.87+156C=
XM_005246277.2:c.87+156C=	XP_005246334.1:n.87+156C=
XM_005246280.2:c.87+156C=	XP_005246337.1:n.87+156C=
XM_006712245.2:c.87+156C=	XP_006712308.1:n.87+156C=
XM_011510555.1:c.87+156C=	XP_011508857.1:n.87+156C=
XR_241280.2:n.225+156C=
XM_005246277.3:c.87+156C=	XP_005246334.1:n.87+156C=
XM_005246280.3:c.87+156C=	XP_005246337.1:n.87+156C=
XM_006712245.3:c.87+156C=	XP_006712308.1:n.87+156C=
XM_017003295.1:c.87+156C=	XP_016858784.1:n.87+156C=
XR_001738601.1:n.225+156C=
XR_241280.3:n.225+156C=
NM_000091.5:c.87+156C= MANE Select	NP_000082.2:n.87+156C=