Canonical Allele Identifier: CA1332796063

Gene: COL4A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227164812A= , CM000664.2:g.227164812A=	GRCh38
NC_000002.11:g.228029528A= , CM000664.1:g.228029528A=	GRCh37
NC_000002.10:g.227737772A=	NCBI36
NG_011591.1:g.5248A= , LRG_230:g.5248A=
NG_011592.1:g.4748T= , LRG_231:g.4748T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396578.8:c.86A= MANE Select	ENSP00000379823.3:p.Lys29=
ENST00000396578.7:c.86A=	ENSP00000379823.3:p.Lys29=
NM_000091.4:c.86A= , LRG_230t1:c.86A=	NP_000082.2:p.Lys29=
XM_005246276.2:c.86A=	XP_005246333.1:p.Lys29=
XM_005246277.2:c.86A=	XP_005246334.1:p.Lys29=
XM_005246280.2:c.86A=	XP_005246337.1:p.Lys29=
XM_006712245.2:c.86A=	XP_006712308.1:p.Lys29=
XM_011510555.1:c.86A=	XP_011508857.1:p.Lys29=
XR_241280.2:n.224A=
XM_005246277.3:c.86A=	XP_005246334.1:p.Lys29=
XM_005246280.3:c.86A=	XP_005246337.1:p.Lys29=
XM_006712245.3:c.86A=	XP_006712308.1:p.Lys29=
XM_017003295.1:c.86A=	XP_016858784.1:p.Lys29=
XR_001738601.1:n.224A=
XR_241280.3:n.224A=
NM_000091.5:c.86A= MANE Select	NP_000082.2:p.Lys29=