Canonical Allele Identifier: CA2663403305
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227266376_227266377del , CM000664.2:g.227266376_227266377del GRCh38
NC_000002.11:g.228131092_228131093del , CM000664.1:g.228131092_228131093del GRCh37
NC_000002.10:g.227839336_227839337del NCBI36
NG_011591.1:g.106812_106813del , LRG_230:g.106812_106813del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396578.8:c.1316-41_1316-40del (COL4A3) MANE Select ENSP00000379823.3:n.1316-41_1316-40del
ENST00000396578.7:c.1316-41_1316-40del (COL4A3) ENSP00000379823.3:n.1316-41_1316-40del
NM_000091.4:c.1316-41_1316-40del , LRG_230t1:c.1316-41_1316-40del (COL4A3) NP_000082.2:n.1316-41_1316-40del
NR_102371.1:n.656-437_656-436del (MFF-DT)
XM_005246276.2:c.1316-41_1316-40del (COL4A3) XP_005246333.1:n.1316-41_1316-40del
XM_005246277.2:c.1316-41_1316-40del (COL4A3) XP_005246334.1:n.1316-41_1316-40del
XM_005246280.2:c.1316-41_1316-40del (COL4A3) XP_005246337.1:n.1316-41_1316-40del
XM_006712245.2:c.1316-41_1316-40del (COL4A3) XP_006712308.1:n.1316-41_1316-40del
XM_011510555.1:c.1316-41_1316-40del (COL4A3) XP_011508857.1:n.1316-41_1316-40del
XM_011510556.1:c.77-41_77-40del (COL4A3) XP_011508858.1:n.77-41_77-40del
XR_241280.2:n.1454-41_1454-40del (COL4A3)
XM_005246277.3:c.1316-41_1316-40del (COL4A3) XP_005246334.1:n.1316-41_1316-40del
XM_005246280.3:c.1316-41_1316-40del (COL4A3) XP_005246337.1:n.1316-41_1316-40del
XM_006712245.3:c.1316-41_1316-40del (COL4A3) XP_006712308.1:n.1316-41_1316-40del
XM_011510556.2:c.77-41_77-40del (COL4A3) XP_011508858.1:n.77-41_77-40del
XM_017003295.1:c.1316-41_1316-40del (COL4A3) XP_016858784.1:n.1316-41_1316-40del
XR_001738601.1:n.1454-41_1454-40del (COL4A3)
XR_241280.3:n.1454-41_1454-40del (COL4A3)
NM_000091.5:c.1316-41_1316-40del (COL4A3) MANE Select NP_000082.2:n.1316-41_1316-40del