Canonical Allele Identifier: CA2568366651
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108439958_108439959del , CM000685.2:g.108439958_108439959del GRCh38
NC_000023.10:g.107683188_107683189del , CM000685.1:g.107683188_107683189del GRCh37
NC_000023.9:g.107569844_107569845del NCBI36
NG_011977.1:g.5035_5036del
NG_012059.2:g.4517_4518del
NG_011977.2:g.5035_5036del

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.-168_-167del MANE Select ENSP00000331902.7:n.-168_-167del
ENST00000361603.7:c.-168_-167del ENSP00000354505.2:n.-168_-167del
ENST00000642185.1:c.-168_-167del ENSP00000495101.1:n.-168_-167del
ENST00000328300.10:c.-168_-167del ENSP00000331902.6:n.-168_-167del
ENST00000361603.6:c.-168_-167del ENSP00000354505.2:n.-168_-167del
ENST00000470339.1:n.17_18del
ENST00000477429.1:n.115_116del
NM_000495.4:c.-168_-167del NP_000486.1:n.-168_-167del
NM_033380.2:c.-168_-167del NP_203699.1:n.-168_-167del
XM_005262070.2:c.-168_-167del XP_005262127.1:n.-168_-167del
XM_005262072.3:c.-168_-167del XP_005262129.1:n.-168_-167del
XM_006724616.2:c.-120-48_-120-47del XP_006724679.1:n.-120-48_-120-47del
XM_011530850.1:c.-168_-167del XP_011529152.1:n.-168_-167del
NM_000495.5:c.-168_-167del NP_000486.1:n.-168_-167del
NM_033380.3:c.-168_-167del MANE Select NP_203699.1:n.-168_-167del