Canonical Allele Identifier: CA2580701028
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108591172A= , CM000685.2:g.108591172A= GRCh38
NC_000023.10:g.107834402A= , CM000685.1:g.107834402A= GRCh37
NC_000023.9:g.107721058A= NCBI36
NG_011977.1:g.156249A=
NG_011977.2:g.156249A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.1280A= MANE Select ENSP00000331902.7:p.Gln427=
ENST00000361603.7:c.1280A= ENSP00000354505.2:p.Gln427=
ENST00000328300.10:c.1280A= ENSP00000331902.6:p.Gln427=
ENST00000361603.6:c.1280A= ENSP00000354505.2:p.Gln427=
ENST00000483338.1:n.736A=
NM_000495.4:c.1280A= NP_000486.1:p.Gln427=
NM_033380.2:c.1280A= NP_203699.1:p.Gln427=
XM_005262070.2:c.1280A= XP_005262127.1:p.Gln427=
XM_005262072.3:c.1280A= XP_005262129.1:p.Gln427=
XM_006724616.2:c.1280A= XP_006724679.1:p.Gln427=
XM_011530849.1:c.956A= XP_011529151.1:p.Gln319=
XM_011530850.1:c.1280A= XP_011529152.1:p.Gln427=
XM_011530849.2:c.1295A= XP_011529151.2:p.Gln432=
XM_017029259.2:c.1295A= XP_016884748.1:p.Gln432=
XM_017029260.1:c.1295A= XP_016884749.1:p.Gln432=
XM_017029261.1:c.1295A= XP_016884750.1:p.Gln432=
XM_017029262.2:c.1295A= XP_016884751.1:p.Gln432=
XM_017029263.2:c.-430A= XP_016884752.1:n.-430A=
NM_000495.5:c.1280A= NP_000486.1:p.Gln427=
NM_033380.3:c.1280A= MANE Select NP_203699.1:p.Gln427=