Canonical Allele Identifier: CA765678843

Gene: COL4A3 MFF-DT

Linked Data

• dbSNP Id: rs1308269942
• MyVariant Identifiers: chr2:g.228176767G>A (hg19) ; chr2:g.227312051G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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