Canonical Allele Identifier: CA2450721567
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108694808T= , CM000685.2:g.108694808T= GRCh38
NC_000023.10:g.107938038T= , CM000685.1:g.107938038T= GRCh37
NC_000023.9:g.107824694T= NCBI36
NG_011977.1:g.259885T=
NG_011977.2:g.259885T=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.4708T= MANE Select ENSP00000331902.7:p.Cys1570=
ENST00000361603.7:c.4690T= ENSP00000354505.2:p.Cys1564=
ENST00000510690.2:n.1202T=
ENST00000644079.1:n.1194T=
ENST00000328300.10:c.4708T= ENSP00000331902.6:p.Cys1570=
ENST00000361603.6:c.4690T= ENSP00000354505.2:p.Cys1564=
ENST00000504541.1:c.106T= ENSP00000424845.1:p.Cys36=
ENST00000515658.1:c.325-1489T=
NM_000495.4:c.4690T= NP_000486.1:p.Cys1564=
NM_033380.2:c.4708T= NP_203699.1:p.Cys1570=
XM_005262070.2:c.4699T= XP_005262127.1:p.Cys1567=
XM_006724616.2:c.4708T= XP_006724679.1:p.Cys1570=
XM_011530849.1:c.4384T= XP_011529151.1:p.Cys1462=
XM_011530851.1:c.2281T= XP_011529153.1:p.Cys761=
XM_011530849.2:c.4723T= XP_011529151.2:p.Cys1575=
XM_017029259.2:c.4714T= XP_016884748.1:p.Cys1572=
XM_017029260.1:c.4705T= XP_016884749.1:p.Cys1569=
XM_017029263.2:c.3043T= XP_016884752.1:p.Cys1015=
NM_000495.5:c.4690T= NP_000486.1:p.Cys1564=
NM_033380.3:c.4708T= MANE Select NP_203699.1:p.Cys1570=