Canonical Allele Identifier: CA431501713

Gene: COL4A3 MFF-DT

Linked Data

• MyVariant Identifiers: chr2:g.228145170A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227280454A>T , CM000664.2:g.227280454A>T	GRCh38
NC_000002.11:g.228145170A>T , CM000664.1:g.228145170A>T	GRCh37
NC_000002.10:g.227853414A>T	NCBI36
NG_011591.1:g.120890A>T , LRG_230:g.120890A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396578.8:c.2238A>T (COL4A3) MANE Select	ENSP00000379823.3:p.Val746=
ENST00000396578.7:c.2238A>T (COL4A3)	ENSP00000379823.3:p.Val746=
NM_000091.4:c.2238A>T , LRG_230t1:c.2238A>T (COL4A3)	NP_000082.2:p.Val746=
NR_102371.1:n.330-879T>A (MFF-DT)
XM_005246276.2:c.2238A>T (COL4A3)	XP_005246333.1:p.Val746=
XM_005246277.2:c.2133A>T (COL4A3)	XP_005246334.1:p.Val711=
XM_005246280.2:c.2238A>T (COL4A3)	XP_005246337.1:p.Val746=
XM_006712245.2:c.2238A>T (COL4A3)	XP_006712308.1:p.Val746=
XM_011510555.1:c.2238A>T (COL4A3)	XP_011508857.1:p.Val746=
XM_011510556.1:c.999A>T (COL4A3)	XP_011508858.1:p.Val333=
XR_241280.2:n.2376A>T (COL4A3)
XM_005246277.3:c.2133A>T (COL4A3)	XP_005246334.1:p.Val711=
XM_005246280.3:c.2238A>T (COL4A3)	XP_005246337.1:p.Val746=
XM_006712245.3:c.2238A>T (COL4A3)	XP_006712308.1:p.Val746=
XM_011510556.2:c.999A>T (COL4A3)	XP_011508858.1:p.Val333=
XM_017003295.1:c.2238A>T (COL4A3)	XP_016858784.1:p.Val746=
XR_001738601.1:n.2376A>T (COL4A3)
XR_241280.3:n.2376A>T (COL4A3)
NM_000091.5:c.2238A>T (COL4A3) MANE Select	NP_000082.2:p.Val746=