Canonical Allele Identifier: CA2822894776

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108595695_108595696insGTATAAGATCAACAACAAAC , CM000685.2:g.108595695_108595696insGTATAAGATCAACAACAAAC	GRCh38
NC_000023.10:g.107838925_107838926insGTATAAGATCAACAACAAAC , CM000685.1:g.107838925_107838926insGTATAAGATCAACAACAAAC	GRCh37
NC_000023.9:g.107725581_107725582insGTATAAGATCAACAACAAAC	NCBI36
NG_011977.1:g.160772_160773insGTATAAGATCAACAACAAAC
NG_011977.2:g.160772_160773insGTATAAGATCAACAACAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.1516+94_1516+95insGTATAAGATCAACAACAAAC MANE Select	ENSP00000331902.7:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
ENST00000361603.7:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	ENSP00000354505.2:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
ENST00000328300.10:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	ENSP00000331902.6:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
ENST00000361603.6:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	ENSP00000354505.2:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
ENST00000483338.1:n.972+94_972+95insGTATAAGATCAACAACAAAC
NM_000495.4:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	NP_000486.1:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
NM_033380.2:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	NP_203699.1:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
XM_005262070.2:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	XP_005262127.1:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
XM_005262072.3:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	XP_005262129.1:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
XM_006724616.2:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	XP_006724679.1:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
XM_011530849.1:c.1192+94_1192+95insGTATAAGATCAACAACAAAC	XP_011529151.1:n.1192+94_1192+95insGTATAAGATCAACAACAAAC
XM_011530850.1:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	XP_011529152.1:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
XM_011530849.2:c.1531+94_1531+95insGTATAAGATCAACAACAAAC	XP_011529151.2:n.1531+94_1531+95insGTATAAGATCAACAACAAAC
XM_017029259.2:c.1531+94_1531+95insGTATAAGATCAACAACAAAC	XP_016884748.1:n.1531+94_1531+95insGTATAAGATCAACAACAAAC
XM_017029260.1:c.1531+94_1531+95insGTATAAGATCAACAACAAAC	XP_016884749.1:n.1531+94_1531+95insGTATAAGATCAACAACAAAC
XM_017029261.1:c.1531+94_1531+95insGTATAAGATCAACAACAAAC	XP_016884750.1:n.1531+94_1531+95insGTATAAGATCAACAACAAAC
XM_017029262.2:c.1531+94_1531+95insGTATAAGATCAACAACAAAC	XP_016884751.1:n.1531+94_1531+95insGTATAAGATCAACAACAAAC
XM_017029263.2:c.-150+94_-150+95insGTATAAGATCAACAACAAAC	XP_016884752.1:n.-150+94_-150+95insGTATAAGATCAACAACAAAC
NM_000495.5:c.1516+94_1516+95insGTATAAGATCAACAACAAAC	NP_000486.1:n.1516+94_1516+95insGTATAAGATCAACAACAAAC
NM_033380.3:c.1516+94_1516+95insGTATAAGATCAACAACAAAC MANE Select	NP_203699.1:n.1516+94_1516+95insGTATAAGATCAACAACAAAC