Canonical Allele Identifier: CA2822895082
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108580773_108580774insCCAAACACACCCAACAC , CM000685.2:g.108580773_108580774insCCAAACACACCCAACAC GRCh38
NC_000023.10:g.107824003_107824004insCCAAACACACCCAACAC , CM000685.1:g.107824003_107824004insCCAAACACACCCAACAC GRCh37
NC_000023.9:g.107710659_107710660insCCAAACACACCCAACAC NCBI36
NG_011977.1:g.145850_145851insCCAAACACACCCAACAC
NG_011977.2:g.145850_145851insCCAAACACACCCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.891+35_891+36insCCAAACACACCCAACAC MANE Select ENSP00000331902.7:n.891+35_891+36insCCAAACACACCCAACAC
ENST00000361603.7:c.891+35_891+36insCCAAACACACCCAACAC ENSP00000354505.2:n.891+35_891+36insCCAAACACACCCAACAC
ENST00000328300.10:c.891+35_891+36insCCAAACACACCCAACAC ENSP00000331902.6:n.891+35_891+36insCCAAACACACCCAACAC
ENST00000361603.6:c.891+35_891+36insCCAAACACACCCAACAC ENSP00000354505.2:n.891+35_891+36insCCAAACACACCCAACAC
NM_000495.4:c.891+35_891+36insCCAAACACACCCAACAC NP_000486.1:n.891+35_891+36insCCAAACACACCCAACAC
NM_033380.2:c.891+35_891+36insCCAAACACACCCAACAC NP_203699.1:n.891+35_891+36insCCAAACACACCCAACAC
XM_005262070.2:c.891+35_891+36insCCAAACACACCCAACAC XP_005262127.1:n.891+35_891+36insCCAAACACACCCAACAC
XM_005262072.3:c.891+35_891+36insCCAAACACACCCAACAC XP_005262129.1:n.891+35_891+36insCCAAACACACCCAACAC
XM_006724616.2:c.891+35_891+36insCCAAACACACCCAACAC XP_006724679.1:n.891+35_891+36insCCAAACACACCCAACAC
XM_011530849.1:c.567+35_567+36insCCAAACACACCCAACAC XP_011529151.1:n.567+35_567+36insCCAAACACACCCAACAC
XM_011530850.1:c.891+35_891+36insCCAAACACACCCAACAC XP_011529152.1:n.891+35_891+36insCCAAACACACCCAACAC
XM_011530849.2:c.906+35_906+36insCCAAACACACCCAACAC XP_011529151.2:n.906+35_906+36insCCAAACACACCCAACAC
XM_017029259.2:c.906+35_906+36insCCAAACACACCCAACAC XP_016884748.1:n.906+35_906+36insCCAAACACACCCAACAC
XM_017029260.1:c.906+35_906+36insCCAAACACACCCAACAC XP_016884749.1:n.906+35_906+36insCCAAACACACCCAACAC
XM_017029261.1:c.906+35_906+36insCCAAACACACCCAACAC XP_016884750.1:n.906+35_906+36insCCAAACACACCCAACAC
XM_017029262.2:c.906+35_906+36insCCAAACACACCCAACAC XP_016884751.1:n.906+35_906+36insCCAAACACACCCAACAC
NM_000495.5:c.891+35_891+36insCCAAACACACCCAACAC NP_000486.1:n.891+35_891+36insCCAAACACACCCAACAC
NM_033380.3:c.891+35_891+36insCCAAACACACCCAACAC MANE Select NP_203699.1:n.891+35_891+36insCCAAACACACCCAACAC