Canonical Allele Identifier: CA2450715778
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108677568C= , CM000685.2:g.108677568C= GRCh38
NC_000023.10:g.107920798C= , CM000685.1:g.107920798C= GRCh37
NC_000023.9:g.107807454C= NCBI36
NG_011977.1:g.242645C=
NG_011977.2:g.242645C=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.3877C= MANE Select ENSP00000331902.7:p.Pro1293=
ENST00000361603.7:c.3859C= ENSP00000354505.2:p.Pro1287=
ENST00000510690.2:n.371C=
ENST00000328300.10:c.3877C= ENSP00000331902.6:p.Pro1293=
ENST00000361603.6:c.3859C= ENSP00000354505.2:p.Pro1287=
ENST00000489230.1:n.280C=
ENST00000510690.1:n.371C=
NM_000495.4:c.3859C= NP_000486.1:p.Pro1287=
NM_033380.2:c.3877C= NP_203699.1:p.Pro1293=
XM_005262070.2:c.3868C= XP_005262127.1:p.Pro1290=
XM_006724616.2:c.3877C= XP_006724679.1:p.Pro1293=
XM_011530849.1:c.3553C= XP_011529151.1:p.Pro1185=
XM_011530851.1:c.1450C= XP_011529153.1:p.Pro484=
XM_011530849.2:c.3892C= XP_011529151.2:p.Pro1298=
XM_017029259.2:c.3883C= XP_016884748.1:p.Pro1295=
XM_017029260.1:c.3874C= XP_016884749.1:p.Pro1292=
XM_017029261.1:c.3892C= XP_016884750.1:p.Pro1298=
XM_017029263.2:c.2212C= XP_016884752.1:p.Pro738=
NM_000495.5:c.3859C= NP_000486.1:p.Pro1287=
NM_033380.3:c.3877C= MANE Select NP_203699.1:p.Pro1293=