Canonical Allele Identifier: CA2694442776
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108681038_108681046del , CM000685.2:g.108681038_108681046del GRCh38
NC_000023.10:g.107924268_107924276del , CM000685.1:g.107924268_107924276del GRCh37
NC_000023.9:g.107810924_107810932del NCBI36
NG_011977.1:g.246115_246123del
NG_011977.2:g.246115_246123del

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4087+82_4087+90del MANE Select ENSP00000331902.7:n.4087+82_4087+90del
ENST00000361603.7:c.4069+82_4069+90del ENSP00000354505.2:n.4069+82_4069+90del
ENST00000510690.2:n.581+82_581+90del
ENST00000328300.10:c.4087+82_4087+90del ENSP00000331902.6:n.4087+82_4087+90del
ENST00000361603.6:c.4069+82_4069+90del ENSP00000354505.2:n.4069+82_4069+90del
ENST00000489230.1:n.490+82_490+90del
NM_000495.4:c.4069+82_4069+90del NP_000486.1:n.4069+82_4069+90del
NM_033380.2:c.4087+82_4087+90del NP_203699.1:n.4087+82_4087+90del
XM_005262070.2:c.4078+82_4078+90del XP_005262127.1:n.4078+82_4078+90del
XM_006724616.2:c.4087+82_4087+90del XP_006724679.1:n.4087+82_4087+90del
XM_011530849.1:c.3763+82_3763+90del XP_011529151.1:n.3763+82_3763+90del
XM_011530851.1:c.1660+82_1660+90del XP_011529153.1:n.1660+82_1660+90del
XM_011530849.2:c.4102+82_4102+90del XP_011529151.2:n.4102+82_4102+90del
XM_017029259.2:c.4093+82_4093+90del XP_016884748.1:n.4093+82_4093+90del
XM_017029260.1:c.4084+82_4084+90del XP_016884749.1:n.4084+82_4084+90del
XM_017029263.2:c.2422+82_2422+90del XP_016884752.1:n.2422+82_2422+90del
NM_000495.5:c.4069+82_4069+90del NP_000486.1:n.4069+82_4069+90del
NM_033380.3:c.4087+82_4087+90del MANE Select NP_203699.1:n.4087+82_4087+90del