Canonical Allele Identifier: CA2450717238
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108681844G= , CM000685.2:g.108681844G= GRCh38
NC_000023.10:g.107925074G= , CM000685.1:g.107925074G= GRCh37
NC_000023.9:g.107811730G= NCBI36
NG_011977.1:g.246921G=
NG_011977.2:g.246921G=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.4172G= MANE Select ENSP00000331902.7:p.Gly1391=
ENST00000361603.7:c.4154G= ENSP00000354505.2:p.Gly1385=
ENST00000510690.2:n.666G=
ENST00000328300.10:c.4172G= ENSP00000331902.6:p.Gly1391=
ENST00000361603.6:c.4154G= ENSP00000354505.2:p.Gly1385=
ENST00000489230.1:n.575G=
NM_000495.4:c.4154G= NP_000486.1:p.Gly1385=
NM_033380.2:c.4172G= NP_203699.1:p.Gly1391=
XM_005262070.2:c.4163G= XP_005262127.1:p.Gly1388=
XM_006724616.2:c.4172G= XP_006724679.1:p.Gly1391=
XM_011530849.1:c.3848G= XP_011529151.1:p.Gly1283=
XM_011530851.1:c.1745G= XP_011529153.1:p.Gly582=
XM_011530849.2:c.4187G= XP_011529151.2:p.Gly1396=
XM_017029259.2:c.4178G= XP_016884748.1:p.Gly1393=
XM_017029260.1:c.4169G= XP_016884749.1:p.Gly1390=
XM_017029263.2:c.2507G= XP_016884752.1:p.Gly836=
NM_000495.5:c.4154G= NP_000486.1:p.Gly1385=
NM_033380.3:c.4172G= MANE Select NP_203699.1:p.Gly1391=