Canonical Allele Identifier: CA1043065320
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Linked Data

dbSNP Id: rs2070261379

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227257514T>C , CM000664.2:g.227257514T>C GRCh38
NC_000002.11:g.228122230T>C , CM000664.1:g.228122230T>C GRCh37
NC_000002.10:g.227830474T>C NCBI36
NG_011591.1:g.97950T>C , LRG_230:g.97950T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396578.8:c.988-89T>C (COL4A3) MANE Select ENSP00000379823.3:n.988-89T>C
ENST00000396578.7:c.988-89T>C (COL4A3) ENSP00000379823.3:n.988-89T>C
NM_000091.4:c.988-89T>C , LRG_230t1:c.988-89T>C (COL4A3) NP_000082.2:n.988-89T>C
NR_102371.1:n.1592+1664A>G (MFF-DT)
XM_005246276.2:c.988-89T>C (COL4A3) XP_005246333.1:n.988-89T>C
XM_005246277.2:c.988-89T>C (COL4A3) XP_005246334.1:n.988-89T>C
XM_005246280.2:c.988-89T>C (COL4A3) XP_005246337.1:n.988-89T>C
XM_006712245.2:c.988-89T>C (COL4A3) XP_006712308.1:n.988-89T>C
XM_011510555.1:c.988-89T>C (COL4A3) XP_011508857.1:n.988-89T>C
XM_011510556.1:c.-248-89T>C (COL4A3) XP_011508858.1:n.-248-89T>C
XR_241280.2:n.1126-89T>C (COL4A3)
XM_005246277.3:c.988-89T>C (COL4A3) XP_005246334.1:n.988-89T>C
XM_005246280.3:c.988-89T>C (COL4A3) XP_005246337.1:n.988-89T>C
XM_006712245.3:c.988-89T>C (COL4A3) XP_006712308.1:n.988-89T>C
XM_011510556.2:c.-248-89T>C (COL4A3) XP_011508858.1:n.-248-89T>C
XM_017003295.1:c.988-89T>C (COL4A3) XP_016858784.1:n.988-89T>C
XR_001738601.1:n.1126-89T>C (COL4A3)
XR_241280.3:n.1126-89T>C (COL4A3)
NM_000091.5:c.988-89T>C (COL4A3) MANE Select NP_000082.2:n.988-89T>C