Canonical Allele Identifier: CA350866774

Gene: COL4A3 MFF-DT

Linked Data

• MyVariant Identifiers: chr2:g.228176536T>A (hg19) ; chr2:g.227311820T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227311820T>A , CM000664.2:g.227311820T>A	GRCh38
NC_000002.11:g.228176536T>A , CM000664.1:g.228176536T>A	GRCh37
NC_000002.10:g.227884780T>A	NCBI36
NG_011591.1:g.152256T>A , LRG_230:g.152256T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.2221T>A (COL4A3)
ENST00000682257.1:n.185T>A (COL4A3)
ENST00000682970.1:n.261T>A (COL4A3)
ENST00000683077.1:n.1902T>A (COL4A3)
ENST00000684413.1:n.2530T>A (COL4A3)
ENST00000684724.1:n.384T>A (COL4A3)
ENST00000396578.8:c.4963T>A (COL4A3) MANE Select	ENSP00000379823.3:p.Leu1655Ile
ENST00000469504.2:c.756T>A (COL4A3)	ENSP00000493493.1:n.756T>A
ENST00000643388.1:c.476T>A (COL4A3)	ENSP00000495177.1:p.Ile159Asn
ENST00000396578.7:c.4963T>A (COL4A3)	ENSP00000379823.3:p.Leu1655Ile
ENST00000469504.1:n.471T>A (COL4A3)
NM_000091.4:c.4963T>A , LRG_230t1:c.4963T>A (COL4A3)	NP_000082.2:p.Leu1655Ile
NR_102371.1:n.48-6165A>T (MFF-DT)
XM_005246276.2:c.4790T>A (COL4A3)	XP_005246333.1:p.Ile1597Asn
XM_005246277.2:c.4858T>A (COL4A3)	XP_005246334.1:p.Leu1620Ile
XM_011510556.1:c.3724T>A (COL4A3)	XP_011508858.1:p.Leu1242Ile
XR_241280.2:n.4923T>A (COL4A3)
XM_005246277.3:c.4858T>A (COL4A3)	XP_005246334.1:p.Leu1620Ile
XM_011510556.2:c.3724T>A (COL4A3)	XP_011508858.1:p.Leu1242Ile
XR_241280.3:n.4923T>A (COL4A3)
NM_000091.5:c.4963T>A (COL4A3) MANE Select	NP_000082.2:p.Leu1655Ile