Canonical Allele Identifier: CA414132881
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108695380C>G , CM000685.2:g.108695380C>G GRCh38
NC_000023.10:g.107938610C>G , CM000685.1:g.107938610C>G GRCh37
NC_000023.9:g.107825266C>G NCBI36
NG_011977.1:g.260457C>G
NG_011977.2:g.260457C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4935C>G MANE Select ENSP00000331902.7:p.Asn1645Lys
ENST00000361603.7:c.4917C>G ENSP00000354505.2:p.Asn1639Lys
ENST00000510690.2:n.1429C>G
ENST00000644079.1:n.1766C>G
ENST00000328300.10:c.4935C>G ENSP00000331902.6:p.Asn1645Lys
ENST00000361603.6:c.4917C>G ENSP00000354505.2:p.Asn1639Lys
ENST00000504541.1:c.219+459C>G ENSP00000424845.1:n.219+459C>G
ENST00000515658.1:c.325-917C>G
NM_000495.4:c.4917C>G NP_000486.1:p.Asn1639Lys
NM_033380.2:c.4935C>G NP_203699.1:p.Asn1645Lys
XM_005262070.2:c.4926C>G XP_005262127.1:p.Asn1642Lys
XM_006724616.2:c.4935C>G XP_006724679.1:p.Asn1645Lys
XM_011530849.1:c.4611C>G XP_011529151.1:p.Asn1537Lys
XM_011530851.1:c.2508C>G XP_011529153.1:p.Asn836Lys
XM_011530849.2:c.4950C>G XP_011529151.2:p.Asn1650Lys
XM_017029259.2:c.4941C>G XP_016884748.1:p.Asn1647Lys
XM_017029260.1:c.4932C>G XP_016884749.1:p.Asn1644Lys
XM_017029263.2:c.3270C>G XP_016884752.1:p.Asn1090Lys
NM_000495.5:c.4917C>G NP_000486.1:p.Asn1639Lys
NM_033380.3:c.4935C>G MANE Select NP_203699.1:p.Asn1645Lys