Canonical Allele Identifier: CA431507169
Community Standard Title: NM_000091.5(COL4A3):c.3591A>G (p.Pro1197=)
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227297699A>G , CM000664.2:g.227297699A>G GRCh38
NC_000002.11:g.228162415A>G , CM000664.1:g.228162415A>G GRCh37
NC_000002.10:g.227870659A>G NCBI36
NG_011591.1:g.138135A>G , LRG_230:g.138135A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000091.5:c.3591A>G (COL4A3) MANE Select NP_000082.2:p.Pro1197=
ENST00000396578.8:c.3591A>G (COL4A3) MANE Select ENSP00000379823.3:p.Pro1197=
NM_000091.4:c.3591A>G , LRG_230t1:c.3591A>G (COL4A3) NP_000082.2:p.Pro1197=
NR_102371.1:n.243+7761T>C (MFF-DT)
ENST00000396578.7:c.3591A>G (COL4A3) ENSP00000379823.3:p.Pro1197=
ENST00000468753.5:n.254A>G (COL4A3)
ENST00000471862.1:n.9A>G (COL4A3)
ENST00000471862.2:n.9A>G (COL4A3)
XM_005246276.2:c.3591A>G (COL4A3) XP_005246333.1:p.Pro1197=
XM_005246277.2:c.3486A>G (COL4A3) XP_005246334.1:p.Pro1162=
XM_005246277.3:c.3486A>G (COL4A3) XP_005246334.1:p.Pro1162=
XM_006712245.2:c.*61A>G (COL4A3) XP_006712308.1:n.*61A>G
XM_006712245.3:c.*61A>G (COL4A3) XP_006712308.1:n.*61A>G
XM_011510555.1:c.3591A>G (COL4A3) XP_011508857.1:p.Pro1197=
XM_011510556.1:c.2352A>G (COL4A3) XP_011508858.1:p.Pro784=
XM_011510556.2:c.2352A>G (COL4A3) XP_011508858.1:p.Pro784=
XR_001738601.1:n.4939A>G (COL4A3)
XR_241280.2:n.3729A>G (COL4A3)
XR_241280.3:n.3729A>G (COL4A3)