Canonical Allele Identifier: CA10488968
Gene: COL4A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1086813
ClinVar RCV Id: RCV001404725
dbSNP Id: rs758168827

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108621842C>G , CM000685.2:g.108621842C>G GRCh38
NC_000023.10:g.107865072C>G , CM000685.1:g.107865072C>G GRCh37
NC_000023.9:g.107751728C>G NCBI36
NG_011977.1:g.186919C>G
NG_011977.2:g.186919C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.2717C>G MANE Select ENSP00000331902.7:p.Pro906Arg
ENST00000361603.7:c.2717C>G ENSP00000354505.2:p.Pro906Arg
ENST00000328300.10:c.2717C>G ENSP00000331902.6:p.Pro906Arg
ENST00000361603.6:c.2717C>G ENSP00000354505.2:p.Pro906Arg
ENST00000483338.1:n.2173C>G
NM_000495.4:c.2717C>G NP_000486.1:p.Pro906Arg
NM_033380.2:c.2717C>G NP_203699.1:p.Pro906Arg
XM_005262070.2:c.2717C>G XP_005262127.1:p.Pro906Arg
XM_005262072.3:c.2717C>G XP_005262129.1:p.Pro906Arg
XM_006724616.2:c.2717C>G XP_006724679.1:p.Pro906Arg
XM_011530849.1:c.2393C>G XP_011529151.1:p.Pro798Arg
XM_011530850.1:c.2717C>G XP_011529152.1:p.Pro906Arg
XM_011530851.1:c.290C>G XP_011529153.1:p.Pro97Arg
XM_011530849.2:c.2732C>G XP_011529151.2:p.Pro911Arg
XM_017029259.2:c.2732C>G XP_016884748.1:p.Pro911Arg
XM_017029260.1:c.2732C>G XP_016884749.1:p.Pro911Arg
XM_017029261.1:c.2732C>G XP_016884750.1:p.Pro911Arg
XM_017029262.2:c.2732C>G XP_016884751.1:p.Pro911Arg
XM_017029263.2:c.1052C>G XP_016884752.1:p.Pro351Arg
NM_000495.5:c.2717C>G NP_000486.1:p.Pro906Arg
NM_033380.3:c.2717C>G MANE Select NP_203699.1:p.Pro906Arg