Canonical Allele Identifier: CA2579675643
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108440110del , CM000685.2:g.108440110del GRCh38
NC_000023.10:g.107683340del , CM000685.1:g.107683340del GRCh37
NC_000023.9:g.107569996del NCBI36
NG_011977.1:g.5187del
NG_012059.2:g.4365del
NG_011977.2:g.5187del

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.-16del MANE Select ENSP00000331902.7:n.-16del
ENST00000361603.7:c.-16del ENSP00000354505.2:n.-16del
ENST00000642185.1:c.-16del ENSP00000495101.1:n.-16del
ENST00000328300.10:c.-16del ENSP00000331902.6:n.-16del
ENST00000361603.6:c.-16del ENSP00000354505.2:n.-16del
ENST00000470339.1:n.169del
ENST00000477429.1:n.267del
NM_000495.4:c.-16del NP_000486.1:n.-16del
NM_033380.2:c.-16del NP_203699.1:n.-16del
XM_005262070.2:c.-16del XP_005262127.1:n.-16del
XM_005262072.3:c.-16del XP_005262129.1:n.-16del
XM_006724616.2:c.-16del XP_006724679.1:n.-16del
XM_011530850.1:c.-16del XP_011529152.1:n.-16del
NM_000495.5:c.-16del NP_000486.1:n.-16del
NM_033380.3:c.-16del MANE Select NP_203699.1:n.-16del