Canonical Allele Identifier: CA2695235175
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108440177_108440178del , CM000685.2:g.108440177_108440178del GRCh38
NC_000023.10:g.107683407_107683408del , CM000685.1:g.107683407_107683408del GRCh37
NC_000023.9:g.107570063_107570064del NCBI36
NG_011977.1:g.5254_5255del
NG_012059.2:g.4298_4299del
NG_011977.2:g.5254_5255del

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.52_53del MANE Select ENSP00000331902.7:p.Trp20GlyfsTer19
ENST00000361603.7:c.52_53del ENSP00000354505.2:p.Trp20GlyfsTer19
ENST00000642185.1:c.52_53del ENSP00000495101.1:p.Trp20GlyfsTer28
ENST00000328300.10:c.52_53del ENSP00000331902.6:p.Trp20GlyfsTer19
ENST00000361603.6:c.52_53del ENSP00000354505.2:p.Trp20GlyfsTer19
ENST00000470339.1:n.236_237del
ENST00000477429.1:n.334_335del
NM_000495.4:c.52_53del NP_000486.1:p.Trp20GlyfsTer19
NM_033380.2:c.52_53del NP_203699.1:p.Trp20GlyfsTer19
XM_005262070.2:c.52_53del XP_005262127.1:p.Trp20GlyfsTer19
XM_005262072.3:c.52_53del XP_005262129.1:p.Trp20GlyfsTer19
XM_006724616.2:c.52_53del XP_006724679.1:p.Trp20GlyfsTer19
XM_011530850.1:c.52_53del XP_011529152.1:p.Trp20GlyfsTer19
NM_000495.5:c.52_53del NP_000486.1:p.Trp20GlyfsTer19
NM_033380.3:c.52_53del MANE Select NP_203699.1:p.Trp20GlyfsTer19