Canonical Allele Identifier: CA258677
Gene: COL4A5 HGNC NCBI

Linked Data

dbSNP Id: rs104886178

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108606894del , CM000685.2:g.108606894del GRCh38
NC_000023.10:g.107850124del , CM000685.1:g.107850124del GRCh37
NC_000023.9:g.107736780del NCBI36
NG_011977.1:g.171971del
NG_011977.2:g.171971del

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.2395+2del MANE Select ENSP00000331902.7:n.2395+2del
ENST00000361603.7:c.2395+2del ENSP00000354505.2:n.2395+2del
ENST00000328300.10:c.2395+2del ENSP00000331902.6:n.2395+2del
ENST00000361603.6:c.2395+2del ENSP00000354505.2:n.2395+2del
ENST00000483338.1:n.1851+2del
NM_000495.4:c.2395+2del NP_000486.1:n.2395+2del
NM_033380.2:c.2395+2del NP_203699.1:n.2395+2del
XM_005262070.2:c.2395+2del XP_005262127.1:n.2395+2del
XM_005262072.3:c.2395+2del XP_005262129.1:n.2395+2del
XM_006724616.2:c.2395+2del XP_006724679.1:n.2395+2del
XM_011530849.1:c.2071+2del XP_011529151.1:n.2071+2del
XM_011530850.1:c.2395+2del XP_011529152.1:n.2395+2del
XM_011530851.1:c.-33+3833del XP_011529153.1:n.-33+3833del
XM_011530849.2:c.2410+2del XP_011529151.2:n.2410+2del
XM_017029259.2:c.2410+2del XP_016884748.1:n.2410+2del
XM_017029260.1:c.2410+2del XP_016884749.1:n.2410+2del
XM_017029261.1:c.2410+2del XP_016884750.1:n.2410+2del
XM_017029262.2:c.2410+2del XP_016884751.1:n.2410+2del
XM_017029263.2:c.730+2del XP_016884752.1:n.730+2del
NM_000495.5:c.2395+2del NP_000486.1:n.2395+2del
NM_033380.3:c.2395+2del MANE Select NP_203699.1:n.2395+2del