Canonical Allele Identifier: CA350865527
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227309227C>G , CM000664.2:g.227309227C>G GRCh38
NC_000002.11:g.228173943C>G , CM000664.1:g.228173943C>G GRCh37
NC_000002.10:g.227882187C>G NCBI36
NG_011591.1:g.149663C>G , LRG_230:g.149663C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.1922C>G (COL4A3)
ENST00000682257.1:n.59C>G (COL4A3)
ENST00000683077.1:n.146C>G (COL4A3)
ENST00000684413.1:n.2231C>G (COL4A3)
ENST00000684724.1:n.85C>G (COL4A3)
ENST00000396578.8:c.4664C>G (COL4A3) MANE Select ENSP00000379823.3:p.Ala1555Gly
ENST00000469504.2:c.457C>G (COL4A3) ENSP00000493493.1:p.Arg153Gly
ENST00000643388.1:c.350C>G (COL4A3) ENSP00000495177.1:p.Ala117Gly
ENST00000396578.7:c.4664C>G (COL4A3) ENSP00000379823.3:p.Ala1555Gly
ENST00000469504.1:n.172C>G (COL4A3)
NM_000091.4:c.4664C>G , LRG_230t1:c.4664C>G (COL4A3) NP_000082.2:p.Ala1555Gly
NR_102371.1:n.48-3572G>C (MFF-DT)
XM_005246276.2:c.4664C>G (COL4A3) XP_005246333.1:p.Ala1555Gly
XM_005246277.2:c.4559C>G (COL4A3) XP_005246334.1:p.Ala1520Gly
XM_011510555.1:c.4664C>G (COL4A3) XP_011508857.1:p.Ala1555Gly
XM_011510556.1:c.3425C>G (COL4A3) XP_011508858.1:p.Ala1142Gly
XR_241280.2:n.4624C>G (COL4A3)
XM_005246277.3:c.4559C>G (COL4A3) XP_005246334.1:p.Ala1520Gly
XM_011510556.2:c.3425C>G (COL4A3) XP_011508858.1:p.Ala1142Gly
XR_241280.3:n.4624C>G (COL4A3)
NM_000091.5:c.4664C>G (COL4A3) MANE Select NP_000082.2:p.Ala1555Gly