Canonical Allele Identifier: CA350863488

Gene: COL4A3 MFF-DT

Linked Data

• dbSNP Id: rs6436669
• MyVariant Identifiers: chr2:g.228113175A>T (hg19) ; chr2:g.227248459A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227248459A>T , CM000664.2:g.227248459A>T	GRCh38
NC_000002.11:g.228113175A>T , CM000664.1:g.228113175A>T	GRCh37
NC_000002.10:g.227821419A>T	NCBI36
NG_011591.1:g.88895A>T , LRG_230:g.88895A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396578.8:c.485A>T (COL4A3) MANE Select	ENSP00000379823.3:p.Glu162Val
ENST00000396578.7:c.485A>T (COL4A3)	ENSP00000379823.3:p.Glu162Val
NM_000091.4:c.485A>T , LRG_230t1:c.485A>T (COL4A3)	NP_000082.2:p.Glu162Val
NR_102371.1:n.1593-10285T>A (MFF-DT)
XM_005246276.2:c.485A>T (COL4A3)	XP_005246333.1:p.Glu162Val
XM_005246277.2:c.485A>T (COL4A3)	XP_005246334.1:p.Glu162Val
XM_005246280.2:c.485A>T (COL4A3)	XP_005246337.1:p.Glu162Val
XM_006712245.2:c.485A>T (COL4A3)	XP_006712308.1:p.Glu162Val
XM_011510555.1:c.485A>T (COL4A3)	XP_011508857.1:p.Glu162Val
XR_241280.2:n.623A>T (COL4A3)
XM_005246277.3:c.485A>T (COL4A3)	XP_005246334.1:p.Glu162Val
XM_005246280.3:c.485A>T (COL4A3)	XP_005246337.1:p.Glu162Val
XM_006712245.3:c.485A>T (COL4A3)	XP_006712308.1:p.Glu162Val
XM_017003295.1:c.485A>T (COL4A3)	XP_016858784.1:p.Glu162Val
XR_001738601.1:n.623A>T (COL4A3)
XR_241280.3:n.623A>T (COL4A3)
NM_000091.5:c.485A>T (COL4A3) MANE Select	NP_000082.2:p.Glu162Val