Canonical Allele Identifier: CA2579677097
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108681694T>A , CM000685.2:g.108681694T>A GRCh38
NC_000023.10:g.107924924T>A , CM000685.1:g.107924924T>A GRCh37
NC_000023.9:g.107811580T>A NCBI36
NG_011977.1:g.246771T>A
NG_011977.2:g.246771T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.4088-66T>A MANE Select ENSP00000331902.7:n.4088-66T>A
ENST00000361603.7:c.4070-66T>A ENSP00000354505.2:n.4070-66T>A
ENST00000510690.2:n.582-66T>A
ENST00000328300.10:c.4088-66T>A ENSP00000331902.6:n.4088-66T>A
ENST00000361603.6:c.4070-66T>A ENSP00000354505.2:n.4070-66T>A
ENST00000489230.1:n.491-66T>A
NM_000495.4:c.4070-66T>A NP_000486.1:n.4070-66T>A
NM_033380.2:c.4088-66T>A NP_203699.1:n.4088-66T>A
XM_005262070.2:c.4079-66T>A XP_005262127.1:n.4079-66T>A
XM_006724616.2:c.4088-66T>A XP_006724679.1:n.4088-66T>A
XM_011530849.1:c.3764-66T>A XP_011529151.1:n.3764-66T>A
XM_011530851.1:c.1661-66T>A XP_011529153.1:n.1661-66T>A
XM_011530849.2:c.4103-66T>A XP_011529151.2:n.4103-66T>A
XM_017029259.2:c.4094-66T>A XP_016884748.1:n.4094-66T>A
XM_017029260.1:c.4085-66T>A XP_016884749.1:n.4085-66T>A
XM_017029263.2:c.2423-66T>A XP_016884752.1:n.2423-66T>A
NM_000495.5:c.4070-66T>A NP_000486.1:n.4070-66T>A
NM_033380.3:c.4088-66T>A MANE Select NP_203699.1:n.4088-66T>A