Canonical Allele Identifier: CA350865468
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

dbSNP Id: rs1574842147

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227309208A>C , CM000664.2:g.227309208A>C GRCh38
NC_000002.11:g.228173924A>C , CM000664.1:g.228173924A>C GRCh37
NC_000002.10:g.227882168A>C NCBI36
NG_011591.1:g.149644A>C , LRG_230:g.149644A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.1903A>C (COL4A3)
ENST00000682257.1:n.40A>C (COL4A3)
ENST00000683077.1:n.127A>C (COL4A3)
ENST00000684413.1:n.2212A>C (COL4A3)
ENST00000684724.1:n.66A>C (COL4A3)
ENST00000396578.8:c.4645A>C (COL4A3) MANE Select ENSP00000379823.3:p.Thr1549Pro
ENST00000469504.2:c.438A>C (COL4A3) ENSP00000493493.1:p.Ala146=
ENST00000643388.1:c.331A>C (COL4A3) ENSP00000495177.1:p.Thr111Pro
ENST00000396578.7:c.4645A>C (COL4A3) ENSP00000379823.3:p.Thr1549Pro
ENST00000469504.1:n.153A>C (COL4A3)
NM_000091.4:c.4645A>C , LRG_230t1:c.4645A>C (COL4A3) NP_000082.2:p.Thr1549Pro
NR_102371.1:n.48-3553T>G (MFF-DT)
XM_005246276.2:c.4645A>C (COL4A3) XP_005246333.1:p.Thr1549Pro
XM_005246277.2:c.4540A>C (COL4A3) XP_005246334.1:p.Thr1514Pro
XM_011510555.1:c.4645A>C (COL4A3) XP_011508857.1:p.Thr1549Pro
XM_011510556.1:c.3406A>C (COL4A3) XP_011508858.1:p.Thr1136Pro
XR_241280.2:n.4605A>C (COL4A3)
XM_005246277.3:c.4540A>C (COL4A3) XP_005246334.1:p.Thr1514Pro
XM_011510556.2:c.3406A>C (COL4A3) XP_011508858.1:p.Thr1136Pro
XR_241280.3:n.4605A>C (COL4A3)
NM_000091.5:c.4645A>C (COL4A3) MANE Select NP_000082.2:p.Thr1549Pro