Canonical Allele Identifier: CA2450722084
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108696361T= , CM000685.2:g.108696361T= GRCh38
NC_000023.10:g.107939591T= , CM000685.1:g.107939591T= GRCh37
NC_000023.9:g.107826247T= NCBI36
NG_011977.1:g.261438T=
NG_011977.2:g.261438T=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.5059T= MANE Select ENSP00000331902.7:p.Cys1687=
ENST00000361603.7:c.5041T= ENSP00000354505.2:p.Cys1681=
ENST00000510690.2:n.1553T=
ENST00000644079.1:n.2747T=
ENST00000328300.10:c.5059T= ENSP00000331902.6:p.Cys1687=
ENST00000361603.6:c.5041T= ENSP00000354505.2:p.Cys1681=
ENST00000504541.1:c.284T= ENSP00000424845.1:n.284T=
ENST00000515658.1:c.389T=
NM_000495.4:c.5041T= NP_000486.1:p.Cys1681=
NM_033380.2:c.5059T= NP_203699.1:p.Cys1687=
XM_005262070.2:c.5050T= XP_005262127.1:p.Cys1684=
XM_006724616.2:c.5059T= XP_006724679.1:p.Cys1687=
XM_011530849.1:c.4735T= XP_011529151.1:p.Cys1579=
XM_011530851.1:c.2632T= XP_011529153.1:p.Cys878=
XM_011530849.2:c.5074T= XP_011529151.2:p.Cys1692=
XM_017029259.2:c.5065T= XP_016884748.1:p.Cys1689=
XM_017029260.1:c.5056T= XP_016884749.1:p.Cys1686=
XM_017029263.2:c.3394T= XP_016884752.1:p.Cys1132=
NM_000495.5:c.5041T= NP_000486.1:p.Cys1681=
NM_033380.3:c.5059T= MANE Select NP_203699.1:p.Cys1687=