Canonical Allele Identifier: CA2580612279
Gene: COL4A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057041
ClinVar RCV Id: RCV001365956
dbSNP Id: rs2147734917

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108563930_108563933del , CM000685.2:g.108563930_108563933del GRCh38
NC_000023.10:g.107807160_107807163del , CM000685.1:g.107807160_107807163del GRCh37
NC_000023.9:g.107693816_107693819del NCBI36
NG_011977.1:g.129007_129010del
NG_011977.2:g.129007_129010del

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.276+4_276+7del
ENST00000361603.7:c.276+4_276+7del
ENST00000328300.10:c.276+4_276+7del
ENST00000361603.6:c.276+4_276+7del
ENST00000470339.1:n.460+4_460+7del
NM_000495.4:c.276+4_276+7del
NM_033380.2:c.276+4_276+7del
XM_005262070.2:c.276+4_276+7del
XM_005262072.3:c.276+4_276+7del
XM_006724616.2:c.276+4_276+7del
XM_011530849.1:c.-49+4_-49+7del
XM_011530850.1:c.276+4_276+7del
XM_011530849.2:c.291+4_291+7del
XM_017029259.2:c.291+4_291+7del
XM_017029260.1:c.291+4_291+7del
XM_017029261.1:c.291+4_291+7del
XM_017029262.2:c.291+4_291+7del
NM_000495.5:c.276+4_276+7del
NM_033380.3:c.276+4_276+7del