Canonical Allele Identifier: CA1332863131

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227312051G= , CM000664.2:g.227312051G=	GRCh38
NC_000002.11:g.228176767G= , CM000664.1:g.228176767G=	GRCh37
NC_000002.10:g.227885011G=	NCBI36
NG_011591.1:g.152487G= , LRG_230:g.152487G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.2452G= (COL4A3)
ENST00000682257.1:n.416G= (COL4A3)
ENST00000682970.1:n.492G= (COL4A3)
ENST00000683077.1:n.2133G= (COL4A3)
ENST00000684413.1:n.2761G= (COL4A3)
ENST00000684724.1:n.615G= (COL4A3)
ENST00000396578.8:c.*181G= (COL4A3) MANE Select	ENSP00000379823.3:n.*181G=
ENST00000396578.7:c.*181G= (COL4A3)	ENSP00000379823.3:n.*181G=
NM_000091.4:c.*181G= , LRG_230t1:c.*181G= (COL4A3)	NP_000082.2:n.*181G=
NR_102371.1:n.48-6396C= (MFF-DT)
XM_005246276.2:c.*107G= (COL4A3)	XP_005246333.1:n.*107G=
XM_005246277.2:c.*181G= (COL4A3)	XP_005246334.1:n.*181G=
XM_011510556.1:c.*181G= (COL4A3)	XP_011508858.1:n.*181G=
XR_241280.2:n.5154G= (COL4A3)
XM_005246277.3:c.*181G= (COL4A3)	XP_005246334.1:n.*181G=
XM_011510556.2:c.*181G= (COL4A3)	XP_011508858.1:n.*181G=
XR_241280.3:n.5154G= (COL4A3)
NM_000091.5:c.*181G= (COL4A3) MANE Select	NP_000082.2:n.*181G=