Canonical Allele Identifier: CA1332835359

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227246658T= , CM000664.2:g.227246658T=	GRCh38
NC_000002.11:g.228111374T= , CM000664.1:g.228111374T=	GRCh37
NC_000002.10:g.227819618T=	NCBI36
NG_011591.1:g.87094T= , LRG_230:g.87094T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396578.8:c.388-27T= (COL4A3) MANE Select	ENSP00000379823.3:n.388-27T=
ENST00000396578.7:c.388-27T= (COL4A3)	ENSP00000379823.3:n.388-27T=
NM_000091.4:c.388-27T= , LRG_230t1:c.388-27T= (COL4A3)	NP_000082.2:n.388-27T=
NR_102371.1:n.1593-8484A= (MFF-DT)
XM_005246276.2:c.388-27T= (COL4A3)	XP_005246333.1:n.388-27T=
XM_005246277.2:c.388-27T= (COL4A3)	XP_005246334.1:n.388-27T=
XM_005246280.2:c.388-27T= (COL4A3)	XP_005246337.1:n.388-27T=
XM_006712245.2:c.388-27T= (COL4A3)	XP_006712308.1:n.388-27T=
XM_011510555.1:c.388-27T= (COL4A3)	XP_011508857.1:n.388-27T=
XR_241280.2:n.526-27T= (COL4A3)
XM_005246277.3:c.388-27T= (COL4A3)	XP_005246334.1:n.388-27T=
XM_005246280.3:c.388-27T= (COL4A3)	XP_005246337.1:n.388-27T=
XM_006712245.3:c.388-27T= (COL4A3)	XP_006712308.1:n.388-27T=
XM_017003295.1:c.388-27T= (COL4A3)	XP_016858784.1:n.388-27T=
XR_001738601.1:n.526-27T= (COL4A3)
XR_241280.3:n.526-27T= (COL4A3)
NM_000091.5:c.388-27T= (COL4A3) MANE Select	NP_000082.2:n.388-27T=