Canonical Allele Identifier: CA334182870
Gene: COL4A5 HGNC NCBI

Linked Data

dbSNP Id: rs104886330
MyVariant Identifiers: chrX:g.107838799_107838835del (hg19) chrX:g.108595569_108595605del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108595570_108595606del , CM000685.2:g.108595570_108595606del GRCh38
NC_000023.10:g.107838800_107838836del , CM000685.1:g.107838800_107838836del GRCh37
NC_000023.9:g.107725456_107725492del NCBI36
NG_011977.1:g.160647_160683del
NG_011977.2:g.160647_160683del

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.1485_1516+5del
ENST00000361603.7:c.1485_1516+5del
ENST00000328300.10:c.1485_1516+5del
ENST00000361603.6:c.1485_1516+5del
ENST00000483338.1:n.941_972+5del
NM_000495.4:c.1485_1516+5del
NM_033380.2:c.1485_1516+5del
XM_005262070.2:c.1485_1516+5del
XM_005262072.3:c.1485_1516+5del
XM_006724616.2:c.1485_1516+5del
XM_011530849.1:c.1161_1192+5del
XM_011530850.1:c.1485_1516+5del
XM_011530849.2:c.1500_1531+5del
XM_017029259.2:c.1500_1531+5del
XM_017029260.1:c.1500_1531+5del
XM_017029261.1:c.1500_1531+5del
XM_017029262.2:c.1500_1531+5del
XM_017029263.2:c.-181_-150+5del
NM_000495.5:c.1485_1516+5del
NM_033380.3:c.1485_1516+5del
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