Canonical Allele Identifier: CA350858952

Gene: COL4A3 MFF-DT

Linked Data

• MyVariant Identifiers: chr2:g.228159760G>C (hg19) ; chr2:g.227295044G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227295044G>C , CM000664.2:g.227295044G>C	GRCh38
NC_000002.11:g.228159760G>C , CM000664.1:g.228159760G>C	GRCh37
NC_000002.10:g.227868004G>C	NCBI36
NG_011591.1:g.135480G>C , LRG_230:g.135480G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396578.8:c.3499G>C (COL4A3) MANE Select	ENSP00000379823.3:p.Gly1167Arg
ENST00000396578.7:c.3499G>C (COL4A3)	ENSP00000379823.3:p.Gly1167Arg
NM_000091.4:c.3499G>C , LRG_230t1:c.3499G>C (COL4A3)	NP_000082.2:p.Gly1167Arg
NR_102371.1:n.243+10416C>G (MFF-DT)
XM_005246276.2:c.3499G>C (COL4A3)	XP_005246333.1:p.Gly1167Arg
XM_005246277.2:c.3394G>C (COL4A3)	XP_005246334.1:p.Gly1132Arg
XM_006712245.2:c.3499G>C (COL4A3)	XP_006712308.1:p.Gly1167Arg
XM_011510555.1:c.3499G>C (COL4A3)	XP_011508857.1:p.Gly1167Arg
XM_011510556.1:c.2260G>C (COL4A3)	XP_011508858.1:p.Gly754Arg
XR_241280.2:n.3637G>C (COL4A3)
XM_005246277.3:c.3394G>C (COL4A3)	XP_005246334.1:p.Gly1132Arg
XM_006712245.3:c.3499G>C (COL4A3)	XP_006712308.1:p.Gly1167Arg
XM_011510556.2:c.2260G>C (COL4A3)	XP_011508858.1:p.Gly754Arg
XR_001738601.1:n.3637G>C (COL4A3)
XR_241280.3:n.3637G>C (COL4A3)
NM_000091.5:c.3499G>C (COL4A3) MANE Select	NP_000082.2:p.Gly1167Arg