Canonical Allele Identifier: CA2450722007
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108696138A= , CM000685.2:g.108696138A= GRCh38
NC_000023.10:g.107939368A= , CM000685.1:g.107939368A= GRCh37
NC_000023.9:g.107826024A= NCBI36
NG_011977.1:g.261215A=
NG_011977.2:g.261215A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4995-159A= MANE Select ENSP00000331902.7:n.4995-159A=
ENST00000361603.7:c.4977-159A= ENSP00000354505.2:n.4977-159A=
ENST00000510690.2:n.1489-159A=
ENST00000644079.1:n.2524A=
ENST00000328300.10:c.4995-159A= ENSP00000331902.6:n.4995-159A=
ENST00000361603.6:c.4977-159A= ENSP00000354505.2:n.4977-159A=
ENST00000504541.1:c.220-159A= ENSP00000424845.1:n.220-159A=
ENST00000515658.1:c.325-159A=
NM_000495.4:c.4977-159A= NP_000486.1:n.4977-159A=
NM_033380.2:c.4995-159A= NP_203699.1:n.4995-159A=
XM_005262070.2:c.4986-159A= XP_005262127.1:n.4986-159A=
XM_006724616.2:c.4995-159A= XP_006724679.1:n.4995-159A=
XM_011530849.1:c.4671-159A= XP_011529151.1:n.4671-159A=
XM_011530851.1:c.2568-159A= XP_011529153.1:n.2568-159A=
XM_011530849.2:c.5010-159A= XP_011529151.2:n.5010-159A=
XM_017029259.2:c.5001-159A= XP_016884748.1:n.5001-159A=
XM_017029260.1:c.4992-159A= XP_016884749.1:n.4992-159A=
XM_017029263.2:c.3330-159A= XP_016884752.1:n.3330-159A=
NM_000495.5:c.4977-159A= NP_000486.1:n.4977-159A=
NM_033380.3:c.4995-159A= MANE Select NP_203699.1:n.4995-159A=