Canonical Allele Identifier: CA350865180
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227309006T>G , CM000664.2:g.227309006T>G GRCh38
NC_000002.11:g.228173722T>G , CM000664.1:g.228173722T>G GRCh37
NC_000002.10:g.227881966T>G NCBI36
NG_011591.1:g.149442T>G , LRG_230:g.149442T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.1828T>G (COL4A3)
ENST00000683077.1:n.52T>G (COL4A3)
ENST00000684413.1:n.2010T>G (COL4A3)
ENST00000396578.8:c.4570T>G (COL4A3) MANE Select ENSP00000379823.3:p.Ser1524Ala
ENST00000469504.2:c.434-198T>G (COL4A3) ENSP00000493493.1:n.434-198T>G
ENST00000643388.1:c.256T>G (COL4A3) ENSP00000495177.1:p.Ser86Ala
ENST00000396578.7:c.4570T>G (COL4A3) ENSP00000379823.3:p.Ser1524Ala
ENST00000469504.1:n.149-198T>G (COL4A3)
NM_000091.4:c.4570T>G , LRG_230t1:c.4570T>G (COL4A3) NP_000082.2:p.Ser1524Ala
NR_102371.1:n.48-3351A>C (MFF-DT)
XM_005246276.2:c.4570T>G (COL4A3) XP_005246333.1:p.Ser1524Ala
XM_005246277.2:c.4465T>G (COL4A3) XP_005246334.1:p.Ser1489Ala
XM_011510555.1:c.4570T>G (COL4A3) XP_011508857.1:p.Ser1524Ala
XM_011510556.1:c.3331T>G (COL4A3) XP_011508858.1:p.Ser1111Ala
XR_241280.2:n.4601-198T>G (COL4A3)
XM_005246277.3:c.4465T>G (COL4A3) XP_005246334.1:p.Ser1489Ala
XM_011510556.2:c.3331T>G (COL4A3) XP_011508858.1:p.Ser1111Ala
XR_241280.3:n.4601-198T>G (COL4A3)
NM_000091.5:c.4570T>G (COL4A3) MANE Select NP_000082.2:p.Ser1524Ala