Canonical Allele Identifier: CA431509591
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.228176562G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227311846G>A , CM000664.2:g.227311846G>A GRCh38
NC_000002.11:g.228176562G>A , CM000664.1:g.228176562G>A GRCh37
NC_000002.10:g.227884806G>A NCBI36
NG_011591.1:g.152282G>A , LRG_230:g.152282G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000471862.2:n.2247G>A (COL4A3)
ENST00000682257.1:n.211G>A (COL4A3)
ENST00000682970.1:n.287G>A (COL4A3)
ENST00000683077.1:n.1928G>A (COL4A3)
ENST00000684413.1:n.2556G>A (COL4A3)
ENST00000684724.1:n.410G>A (COL4A3)
ENST00000396578.8:c.4989G>A (COL4A3) MANE Select ENSP00000379823.3:p.Gln1663=
ENST00000469504.2:c.782G>A (COL4A3) ENSP00000493493.1:n.782G>A
ENST00000643388.1:c.502G>A (COL4A3) ENSP00000495177.1:p.Gly168Ser
ENST00000396578.7:c.4989G>A (COL4A3) ENSP00000379823.3:p.Gln1663=
ENST00000469504.1:n.497G>A (COL4A3)
NM_000091.4:c.4989G>A , LRG_230t1:c.4989G>A (COL4A3) NP_000082.2:p.Gln1663=
NR_102371.1:n.48-6191C>T (MFF-DT)
XM_005246276.2:c.4816G>A (COL4A3) XP_005246333.1:p.Gly1606Ser
XM_005246277.2:c.4884G>A (COL4A3) XP_005246334.1:p.Gln1628=
XM_011510556.1:c.3750G>A (COL4A3) XP_011508858.1:p.Gln1250=
XR_241280.2:n.4949G>A (COL4A3)
XM_005246277.3:c.4884G>A (COL4A3) XP_005246334.1:p.Gln1628=
XM_011510556.2:c.3750G>A (COL4A3) XP_011508858.1:p.Gln1250=
XR_241280.3:n.4949G>A (COL4A3)
NM_000091.5:c.4989G>A (COL4A3) MANE Select NP_000082.2:p.Gln1663=