Canonical Allele Identifier: CA2450634681
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108440186_108440199delinsGGGCAGCCTGCAGA , CM000685.2:g.108440186_108440199delinsGGGCAGCCTGCAGA GRCh38
NC_000023.10:g.107683416_107683429delinsGGGCAGCCTGCAGA , CM000685.1:g.107683416_107683429delinsGGGCAGCCTGCAGA GRCh37
NC_000023.9:g.107570072_107570085delinsGGGCAGCCTGCAGA NCBI36
NG_011977.1:g.5263_5276delinsGGGCAGCCTGCAGA
NG_012059.2:g.4276_4289delinsTCTGCAGGCTGCCC
NG_011977.2:g.5263_5276delinsGGGCAGCCTGCAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.61_74delinsGGGCAGCCTGCAGA MANE Select ENSP00000331902.7:p.Gly21=
ENST00000361603.7:c.61_74delinsGGGCAGCCTGCAGA ENSP00000354505.2:p.Gly21=
ENST00000642185.1:c.61_74delinsGGGCAGCCTGCAGA ENSP00000495101.1:p.Gly21=
ENST00000328300.10:c.61_74delinsGGGCAGCCTGCAGA ENSP00000331902.6:p.Gly21=
ENST00000361603.6:c.61_74delinsGGGCAGCCTGCAGA ENSP00000354505.2:p.Gly21=
ENST00000470339.1:n.245_258delinsGGGCAGCCTGCAGA
ENST00000477429.1:n.343_356delinsGGGCAGCCTGCAGA
NM_000495.4:c.61_74delinsGGGCAGCCTGCAGA NP_000486.1:p.Gly21=
NM_033380.2:c.61_74delinsGGGCAGCCTGCAGA NP_203699.1:p.Gly21=
XM_005262070.2:c.61_74delinsGGGCAGCCTGCAGA XP_005262127.1:p.Gly21=
XM_005262072.3:c.61_74delinsGGGCAGCCTGCAGA XP_005262129.1:p.Gly21=
XM_006724616.2:c.61_74delinsGGGCAGCCTGCAGA XP_006724679.1:p.Gly21=
XM_011530850.1:c.61_74delinsGGGCAGCCTGCAGA XP_011529152.1:p.Gly21=
NM_000495.5:c.61_74delinsGGGCAGCCTGCAGA NP_000486.1:p.Gly21=
NM_033380.3:c.61_74delinsGGGCAGCCTGCAGA MANE Select NP_203699.1:p.Gly21=