Canonical Allele Identifier: CA2450712327
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108666531G= , CM000685.2:g.108666531G= GRCh38
NC_000023.10:g.107909761G= , CM000685.1:g.107909761G= GRCh37
NC_000023.9:g.107796417G= NCBI36
NG_011977.1:g.231608G=
NG_011977.2:g.231608G=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.3490G= MANE Select ENSP00000331902.7:p.Gly1164=
ENST00000361603.7:c.3490G= ENSP00000354505.2:p.Gly1164=
ENST00000328300.10:c.3490G= ENSP00000331902.6:p.Gly1164=
ENST00000361603.6:c.3490G= ENSP00000354505.2:p.Gly1164=
NM_000495.4:c.3490G= NP_000486.1:p.Gly1164=
NM_033380.2:c.3490G= NP_203699.1:p.Gly1164=
XM_005262070.2:c.3490G= XP_005262127.1:p.Gly1164=
XM_006724616.2:c.3490G= XP_006724679.1:p.Gly1164=
XM_011530849.1:c.3166G= XP_011529151.1:p.Gly1056=
XM_011530850.1:c.3490G= XP_011529152.1:p.Gly1164=
XM_011530851.1:c.1063G= XP_011529153.1:p.Gly355=
XM_011530849.2:c.3505G= XP_011529151.2:p.Gly1169=
XM_017029259.2:c.3505G= XP_016884748.1:p.Gly1169=
XM_017029260.1:c.3505G= XP_016884749.1:p.Gly1169=
XM_017029261.1:c.3505G= XP_016884750.1:p.Gly1169=
XM_017029262.2:c.3505G= XP_016884751.1:p.Gly1169=
XM_017029263.2:c.1825G= XP_016884752.1:p.Gly609=
NM_000495.5:c.3490G= NP_000486.1:p.Gly1164=
NM_033380.3:c.3490G= MANE Select NP_203699.1:p.Gly1164=