Canonical Allele Identifier: CA2450690321
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108603056C= , CM000685.2:g.108603056C= GRCh38
NC_000023.10:g.107846286C= , CM000685.1:g.107846286C= GRCh37
NC_000023.9:g.107732942C= NCBI36
NG_011977.1:g.168133C=
NG_011977.2:g.168133C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.2239C= MANE Select ENSP00000331902.7:p.Pro747=
ENST00000361603.7:c.2239C= ENSP00000354505.2:p.Pro747=
ENST00000328300.10:c.2239C= ENSP00000331902.6:p.Pro747=
ENST00000361603.6:c.2239C= ENSP00000354505.2:p.Pro747=
ENST00000483338.1:n.1695C=
NM_000495.4:c.2239C= NP_000486.1:p.Pro747=
NM_033380.2:c.2239C= NP_203699.1:p.Pro747=
XM_005262070.2:c.2239C= XP_005262127.1:p.Pro747=
XM_005262072.3:c.2239C= XP_005262129.1:p.Pro747=
XM_006724616.2:c.2239C= XP_006724679.1:p.Pro747=
XM_011530849.1:c.1915C= XP_011529151.1:p.Pro639=
XM_011530850.1:c.2239C= XP_011529152.1:p.Pro747=
XM_011530851.1:c.-38C= XP_011529153.1:n.-38C=
XM_011530849.2:c.2254C= XP_011529151.2:p.Pro752=
XM_017029259.2:c.2254C= XP_016884748.1:p.Pro752=
XM_017029260.1:c.2254C= XP_016884749.1:p.Pro752=
XM_017029261.1:c.2254C= XP_016884750.1:p.Pro752=
XM_017029262.2:c.2254C= XP_016884751.1:p.Pro752=
XM_017029263.2:c.574C= XP_016884752.1:p.Pro192=
NM_000495.5:c.2239C= NP_000486.1:p.Pro747=
NM_033380.3:c.2239C= MANE Select NP_203699.1:p.Pro747=