Canonical Allele Identifier: CA1332723959
Gene: COL4A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227008202C= , CM000664.2:g.227008202C= GRCh38
NC_000002.11:g.227872918C= , CM000664.1:g.227872918C= GRCh37
NC_000002.10:g.227581162C= NCBI36
NG_011592.1:g.161358G= , LRG_231:g.161358G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682098.1:c.227G= ENSP00000508331.1:p.Trp76=
ENST00000396625.5:c.4625G= MANE Select ENSP00000379866.3:p.Trp1542=
ENST00000396625.3:c.4625G= ENSP00000379866.3:p.Trp1542=
NM_000092.4:c.4625G= , LRG_231t1:c.4625G= NP_000083.3:p.Trp1542=
XM_005246281.2:c.4625G= XP_005246338.1:p.Trp1542=
XM_005246282.2:c.4070G= XP_005246339.1:p.Trp1357=
XM_006712246.2:c.4436G= XP_006712309.1:p.Trp1479=
XM_006712249.2:c.4625G= XP_006712312.1:p.Trp1542=
XM_006712252.2:c.4216+13846G= XP_006712315.1:n.4216+13846G=
XM_011510557.1:c.4544G= XP_011508859.1:p.Trp1515=
XM_011510558.1:c.4517G= XP_011508860.1:p.Trp1506=
XM_011510559.1:c.4625G= XP_011508861.1:p.Trp1542=
XM_011510560.1:c.4625G= XP_011508862.1:p.Trp1542=
XM_011510561.1:c.4625G= XP_011508863.1:p.Trp1542=
XM_011510562.1:c.4625G= XP_011508864.1:p.Trp1542=
XM_011510563.1:c.4371G= XP_011508865.1:p.Leu1457=
XM_011510564.1:c.4254G= XP_011508866.1:p.Leu1418=
XM_011510565.1:c.4216+13846G= XP_011508867.1:n.4216+13846G=
XM_011510566.1:c.4216+13846G= XP_011508868.1:n.4216+13846G=
XM_011510567.1:c.4216+13846G= XP_011508869.1:n.4216+13846G=
XM_011510569.1:c.4216+13846G= XP_011508871.1:n.4216+13846G=
XM_011510570.1:c.4216+13846G= XP_011508872.1:n.4216+13846G=
XM_011510571.1:c.4216+13846G= XP_011508873.1:n.4216+13846G=
XM_011510572.1:c.2951G= XP_011508874.1:p.Trp984=
XR_922837.1:n.4935G=
XR_922838.1:n.4935G=
XR_922839.1:n.4526+13846G=
XR_922840.1:n.4526+13846G=
XM_005246281.3:c.4625G= XP_005246338.1:p.Trp1542=
XM_005246282.3:c.4070G= XP_005246339.1:p.Trp1357=
XM_006712246.3:c.4436G= XP_006712309.1:p.Trp1479=
XM_011510557.2:c.4544G= XP_011508859.1:p.Trp1515=
XM_011510558.2:c.4517G= XP_011508860.1:p.Trp1506=
XM_011510559.2:c.4625G= XP_011508861.1:p.Trp1542=
XM_011510560.2:c.4625G= XP_011508862.1:p.Trp1542=
XM_011510561.2:c.4625G= XP_011508863.1:p.Trp1542=
XM_011510562.2:c.4625G= XP_011508864.1:p.Trp1542=
XM_011510565.2:c.4216+13846G= XP_011508867.1:n.4216+13846G=
XM_011510566.2:c.4216+13846G= XP_011508868.1:n.4216+13846G=
XM_011510567.2:c.4216+13846G= XP_011508869.1:n.4216+13846G=
XM_011510569.2:c.4216+13846G= XP_011508871.1:n.4216+13846G=
XM_011510570.2:c.4216+13846G= XP_011508872.1:n.4216+13846G=
XM_011510572.3:c.2951G= XP_011508874.1:p.Trp984=
XM_017003296.1:c.4625G= XP_016858785.1:p.Trp1542=
XM_017003297.1:c.4508G= XP_016858786.1:p.Trp1503=
XM_017003298.1:c.4625G= XP_016858787.1:p.Trp1542=
XM_017003300.1:c.4216+13846G= XP_016858789.1:n.4216+13846G=
XR_001738602.1:n.4951G=
XR_001738603.1:n.4951G=
XR_001738604.1:n.4697G=
XR_001738606.1:n.4542+13846G=
XR_001738607.1:n.4542+13846G=
XR_922837.2:n.4951G=
NM_000092.5:c.4625G= MANE Select NP_000083.3:p.Trp1542=