Canonical Allele Identifier: CA258249
Gene: COL4A5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 587319
ClinVar RCV Id: RCV000021150
dbSNP Id: rs104886053

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108571812del , CM000685.2:g.108571812del GRCh38
NC_000023.10:g.107815042del , CM000685.1:g.107815042del GRCh37
NC_000023.9:g.107701698del NCBI36
NG_011977.1:g.136889del
NG_011977.2:g.136889del

Transcript Alleles

HGVS Amino-acid change
NM_000495.4:c.440del VV
NM_033380.2:c.440del VV
XM_005262070.2:c.440del
XM_005262072.3:c.440del
XM_006724616.2:c.440del
XM_011530849.1:c.116del
XM_011530850.1:c.440del
XM_011530849.2:c.455del
XM_017029259.2:c.455del
XM_017029260.1:c.455del
XM_017029261.1:c.455del
XM_017029262.2:c.455del
ENST00000328300.10:c.440del
ENST00000361603.6:c.440del