Canonical Allele Identifier: CA350862939

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227304099G>A , CM000664.2:g.227304099G>A	GRCh38
NC_000002.11:g.228168815G>A , CM000664.1:g.228168815G>A	GRCh37
NC_000002.10:g.227877059G>A	NCBI36
NG_011591.1:g.144535G>A , LRG_230:g.144535G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000091.5:c.4108G>A (COL4A3) MANE Select	NP_000082.2:p.Gly1370Arg
ENST00000396578.8:c.4108G>A (COL4A3) MANE Select	ENSP00000379823.3:p.Gly1370Arg
NM_000091.4:c.4108G>A , LRG_230t1:c.4108G>A (COL4A3)	NP_000082.2:p.Gly1370Arg
NR_102371.1:n.243+1361C>T (MFF-DT)
ENST00000396578.7:c.4108G>A (COL4A3)	ENSP00000379823.3:p.Gly1370Arg
ENST00000469504.2:c.79G>A (COL4A3)	ENSP00000493493.1:p.Gly27Arg
ENST00000471862.1:n.526G>A (COL4A3)
ENST00000471862.2:n.526G>A (COL4A3)
XM_005246276.2:c.4108G>A (COL4A3)	XP_005246333.1:p.Gly1370Arg
XM_005246277.2:c.4003G>A (COL4A3)	XP_005246334.1:p.Gly1335Arg
XM_005246277.3:c.4003G>A (COL4A3)	XP_005246334.1:p.Gly1335Arg
XM_011510555.1:c.4108G>A (COL4A3)	XP_011508857.1:p.Gly1370Arg
XM_011510556.1:c.2869G>A (COL4A3)	XP_011508858.1:p.Gly957Arg
XM_011510556.2:c.2869G>A (COL4A3)	XP_011508858.1:p.Gly957Arg
XR_241280.2:n.4246G>A (COL4A3)
XR_241280.3:n.4246G>A (COL4A3)