Canonical Allele Identifier: CA2450712846
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108668103T= , CM000685.2:g.108668103T= GRCh38
NC_000023.10:g.107911333T= , CM000685.1:g.107911333T= GRCh37
NC_000023.9:g.107797989T= NCBI36
NG_011977.1:g.233180T=
NG_011977.2:g.233180T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.3605-216T= MANE Select ENSP00000331902.7:n.3605-216T=
ENST00000361603.7:c.3605-216T= ENSP00000354505.2:n.3605-216T=
ENST00000328300.10:c.3605-216T= ENSP00000331902.6:n.3605-216T=
ENST00000361603.6:c.3605-216T= ENSP00000354505.2:n.3605-216T=
NM_000495.4:c.3605-216T= NP_000486.1:n.3605-216T=
NM_033380.2:c.3605-216T= NP_203699.1:n.3605-216T=
XM_005262070.2:c.3605-216T= XP_005262127.1:n.3605-216T=
XM_006724616.2:c.3605-216T= XP_006724679.1:n.3605-216T=
XM_011530849.1:c.3281-216T= XP_011529151.1:n.3281-216T=
XM_011530850.1:c.3605-216T= XP_011529152.1:n.3605-216T=
XM_011530851.1:c.1178-216T= XP_011529153.1:n.1178-216T=
XM_011530849.2:c.3620-216T= XP_011529151.2:n.3620-216T=
XM_017029259.2:c.3620-216T= XP_016884748.1:n.3620-216T=
XM_017029260.1:c.3620-216T= XP_016884749.1:n.3620-216T=
XM_017029261.1:c.3620-216T= XP_016884750.1:n.3620-216T=
XM_017029262.2:c.3620-216T= XP_016884751.1:n.3620-216T=
XM_017029263.2:c.1940-216T= XP_016884752.1:n.1940-216T=
NM_000495.5:c.3605-216T= NP_000486.1:n.3605-216T=
NM_033380.3:c.3605-216T= MANE Select NP_203699.1:n.3605-216T=