Canonical Allele Identifier: CA1332863119
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227312014A= , CM000664.2:g.227312014A= GRCh38
NC_000002.11:g.228176730A= , CM000664.1:g.228176730A= GRCh37
NC_000002.10:g.227884974A= NCBI36
NG_011591.1:g.152450A= , LRG_230:g.152450A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000471862.2:n.2415A= (COL4A3)
ENST00000682257.1:n.379A= (COL4A3)
ENST00000682970.1:n.455A= (COL4A3)
ENST00000683077.1:n.2096A= (COL4A3)
ENST00000684413.1:n.2724A= (COL4A3)
ENST00000684724.1:n.578A= (COL4A3)
ENST00000396578.8:c.*144A= (COL4A3) MANE Select ENSP00000379823.3:n.*144A=
ENST00000396578.7:c.*144A= (COL4A3) ENSP00000379823.3:n.*144A=
NM_000091.4:c.*144A= , LRG_230t1:c.*144A= (COL4A3) NP_000082.2:n.*144A=
NR_102371.1:n.48-6359T= (MFF-DT)
XM_005246276.2:c.*70A= (COL4A3) XP_005246333.1:n.*70A=
XM_005246277.2:c.*144A= (COL4A3) XP_005246334.1:n.*144A=
XM_011510556.1:c.*144A= (COL4A3) XP_011508858.1:n.*144A=
XR_241280.2:n.5117A= (COL4A3)
XM_005246277.3:c.*144A= (COL4A3) XP_005246334.1:n.*144A=
XM_011510556.2:c.*144A= (COL4A3) XP_011508858.1:n.*144A=
XR_241280.3:n.5117A= (COL4A3)
NM_000091.5:c.*144A= (COL4A3) MANE Select NP_000082.2:n.*144A=