Canonical Allele Identifier: CA2822894985
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108626312_108626313insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC , CM000685.2:g.108626312_108626313insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC GRCh38
NC_000023.10:g.107869542_107869543insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC , CM000685.1:g.107869542_107869543insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC GRCh37
NC_000023.9:g.107756198_107756199insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC NCBI36
NG_011977.1:g.191389_191390insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC
NG_011977.2:g.191389_191390insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC MANE Select ENSP00000331902.7:p.Ser1071LeufsTer?
ENST00000361603.7:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC ENSP00000354505.2:p.Ser1071LeufsTer?
ENST00000328300.10:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC ENSP00000331902.6:p.Ser1071LeufsTer?
ENST00000361603.6:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC ENSP00000354505.2:p.Ser1071LeufsTer?
ENST00000483338.1:n.2665_2666insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC
ENST00000505728.1:c.442_443insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC
NM_000495.4:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC NP_000486.1:p.Ser1071LeufsTer?
NM_033380.2:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC NP_203699.1:p.Ser1071LeufsTer?
XM_005262070.2:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_005262127.1:p.Ser1071LeufsTer?
XM_005262072.3:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_005262129.1:p.Ser1071LeufsTer29
XM_006724616.2:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_006724679.1:p.Ser1071LeufsTer?
XM_011530849.1:c.2885_2886insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_011529151.1:p.Ser963LeufsTer?
XM_011530850.1:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_011529152.1:p.Ser1071LeufsTer?
XM_011530851.1:c.782_783insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_011529153.1:p.Ser262LeufsTer?
XM_011530849.2:c.3224_3225insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_011529151.2:p.Ser1076LeufsTer?
XM_017029259.2:c.3224_3225insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_016884748.1:p.Ser1076LeufsTer?
XM_017029260.1:c.3224_3225insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_016884749.1:p.Ser1076LeufsTer?
XM_017029261.1:c.3224_3225insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_016884750.1:p.Ser1076LeufsTer?
XM_017029262.2:c.3224_3225insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_016884751.1:p.Ser1076LeufsTer?
XM_017029263.2:c.1544_1545insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC XP_016884752.1:p.Ser516LeufsTer?
NM_000495.5:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC NP_000486.1:p.Ser1071LeufsTer?
NM_033380.3:c.3209_3210insACTGGTGACACTGGGCAAAAAGGAGACAAGGGCGACAAAGGCGATAC MANE Select NP_203699.1:p.Ser1071LeufsTer?