Canonical Allele Identifier: CA1332840255
Gene: COL4A3 HGNC NCBI
MFF-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227257637_227257638delinsGT , CM000664.2:g.227257637_227257638delinsGT GRCh38
NC_000002.11:g.228122353_228122354delinsGT , CM000664.1:g.228122353_228122354delinsGT GRCh37
NC_000002.10:g.227830597_227830598delinsGT NCBI36
NG_011591.1:g.98073_98074delinsGT , LRG_230:g.98073_98074delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000396578.8:c.1022_1023delinsGT (COL4A3) MANE Select ENSP00000379823.3:p.Arg341=
ENST00000396578.7:c.1022_1023delinsGT (COL4A3) ENSP00000379823.3:p.Arg341=
NM_000091.4:c.1022_1023delinsGT , LRG_230t1:c.1022_1023delinsGT (COL4A3) NP_000082.2:p.Arg341=
NR_102371.1:n.1592+1540_1592+1541delinsAC (MFF-DT)
XM_005246276.2:c.1022_1023delinsGT (COL4A3) XP_005246333.1:p.Arg341=
XM_005246277.2:c.1022_1023delinsGT (COL4A3) XP_005246334.1:p.Arg341=
XM_005246280.2:c.1022_1023delinsGT (COL4A3) XP_005246337.1:p.Arg341=
XM_006712245.2:c.1022_1023delinsGT (COL4A3) XP_006712308.1:p.Arg341=
XM_011510555.1:c.1022_1023delinsGT (COL4A3) XP_011508857.1:p.Arg341=
XM_011510556.1:c.-214_-213delinsGT (COL4A3) XP_011508858.1:n.-214_-213delinsGT
XR_241280.2:n.1160_1161delinsGT (COL4A3)
XM_005246277.3:c.1022_1023delinsGT (COL4A3) XP_005246334.1:p.Arg341=
XM_005246280.3:c.1022_1023delinsGT (COL4A3) XP_005246337.1:p.Arg341=
XM_006712245.3:c.1022_1023delinsGT (COL4A3) XP_006712308.1:p.Arg341=
XM_011510556.2:c.-214_-213delinsGT (COL4A3) XP_011508858.1:n.-214_-213delinsGT
XM_017003295.1:c.1022_1023delinsGT (COL4A3) XP_016858784.1:p.Arg341=
XR_001738601.1:n.1160_1161delinsGT (COL4A3)
XR_241280.3:n.1160_1161delinsGT (COL4A3)
NM_000091.5:c.1022_1023delinsGT (COL4A3) MANE Select NP_000082.2:p.Arg341=