Canonical Allele Identifier: CA431509502
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.228176520T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227311804T>C , CM000664.2:g.227311804T>C GRCh38
NC_000002.11:g.228176520T>C , CM000664.1:g.228176520T>C GRCh37
NC_000002.10:g.227884764T>C NCBI36
NG_011591.1:g.152240T>C , LRG_230:g.152240T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2205T>C (COL4A3)
ENST00000682257.1:n.169T>C (COL4A3)
ENST00000682970.1:n.245T>C (COL4A3)
ENST00000683077.1:n.1886T>C (COL4A3)
ENST00000684413.1:n.2514T>C (COL4A3)
ENST00000684724.1:n.368T>C (COL4A3)
ENST00000396578.8:c.4947T>C (COL4A3) MANE Select ENSP00000379823.3:p.Thr1649=
ENST00000469504.2:c.740T>C (COL4A3) ENSP00000493493.1:n.740T>C
ENST00000643388.1:c.460T>C (COL4A3) ENSP00000495177.1:p.Cys154Arg
ENST00000396578.7:c.4947T>C (COL4A3) ENSP00000379823.3:p.Thr1649=
ENST00000469504.1:n.455T>C (COL4A3)
NM_000091.4:c.4947T>C , LRG_230t1:c.4947T>C (COL4A3) NP_000082.2:p.Thr1649=
NR_102371.1:n.48-6149A>G (MFF-DT)
XM_005246276.2:c.4774T>C (COL4A3) XP_005246333.1:p.Cys1592Arg
XM_005246277.2:c.4842T>C (COL4A3) XP_005246334.1:p.Thr1614=
XM_011510556.1:c.3708T>C (COL4A3) XP_011508858.1:p.Thr1236=
XR_241280.2:n.4907T>C (COL4A3)
XM_005246277.3:c.4842T>C (COL4A3) XP_005246334.1:p.Thr1614=
XM_011510556.2:c.3708T>C (COL4A3) XP_011508858.1:p.Thr1236=
XR_241280.3:n.4907T>C (COL4A3)
NM_000091.5:c.4947T>C (COL4A3) MANE Select NP_000082.2:p.Thr1649=