Canonical Allele Identifier: CA1332723916
Gene: COL4A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227008120G= , CM000664.2:g.227008120G= GRCh38
NC_000002.11:g.227872836G= , CM000664.1:g.227872836G= GRCh37
NC_000002.10:g.227581080G= NCBI36
NG_011592.1:g.161440C= , LRG_231:g.161440C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682098.1:c.309C= ENSP00000508331.1:p.Cys103=
ENST00000396625.5:c.4707C= MANE Select ENSP00000379866.3:p.Cys1569=
ENST00000396625.3:c.4707C= ENSP00000379866.3:p.Cys1569=
NM_000092.4:c.4707C= , LRG_231t1:c.4707C= NP_000083.3:p.Cys1569=
XM_005246281.2:c.4707C= XP_005246338.1:p.Cys1569=
XM_005246282.2:c.4152C= XP_005246339.1:p.Cys1384=
XM_006712246.2:c.4518C= XP_006712309.1:p.Cys1506=
XM_006712249.2:c.4707C= XP_006712312.1:p.Cys1569=
XM_006712252.2:c.4216+13928C= XP_006712315.1:n.4216+13928C=
XM_011510557.1:c.4626C= XP_011508859.1:p.Cys1542=
XM_011510558.1:c.4599C= XP_011508860.1:p.Cys1533=
XM_011510559.1:c.4707C= XP_011508861.1:p.Cys1569=
XM_011510560.1:c.4707C= XP_011508862.1:p.Cys1569=
XM_011510561.1:c.4707C= XP_011508863.1:p.Cys1569=
XM_011510562.1:c.4707C= XP_011508864.1:p.Cys1569=
XM_011510563.1:c.*40C= XP_011508865.1:n.*40C=
XM_011510564.1:c.*40C= XP_011508866.1:n.*40C=
XM_011510565.1:c.4216+13928C= XP_011508867.1:n.4216+13928C=
XM_011510566.1:c.4216+13928C= XP_011508868.1:n.4216+13928C=
XM_011510567.1:c.4216+13928C= XP_011508869.1:n.4216+13928C=
XM_011510569.1:c.4216+13928C= XP_011508871.1:n.4216+13928C=
XM_011510570.1:c.4216+13928C= XP_011508872.1:n.4216+13928C=
XM_011510571.1:c.4216+13928C= XP_011508873.1:n.4216+13928C=
XM_011510572.1:c.3033C= XP_011508874.1:p.Cys1011=
XR_922837.1:n.5017C=
XR_922838.1:n.5017C=
XR_922839.1:n.4526+13928C=
XR_922840.1:n.4526+13928C=
XM_005246281.3:c.4707C= XP_005246338.1:p.Cys1569=
XM_005246282.3:c.4152C= XP_005246339.1:p.Cys1384=
XM_006712246.3:c.4518C= XP_006712309.1:p.Cys1506=
XM_011510557.2:c.4626C= XP_011508859.1:p.Cys1542=
XM_011510558.2:c.4599C= XP_011508860.1:p.Cys1533=
XM_011510559.2:c.4707C= XP_011508861.1:p.Cys1569=
XM_011510560.2:c.4707C= XP_011508862.1:p.Cys1569=
XM_011510561.2:c.4707C= XP_011508863.1:p.Cys1569=
XM_011510562.2:c.4707C= XP_011508864.1:p.Cys1569=
XM_011510565.2:c.4216+13928C= XP_011508867.1:n.4216+13928C=
XM_011510566.2:c.4216+13928C= XP_011508868.1:n.4216+13928C=
XM_011510567.2:c.4216+13928C= XP_011508869.1:n.4216+13928C=
XM_011510569.2:c.4216+13928C= XP_011508871.1:n.4216+13928C=
XM_011510570.2:c.4216+13928C= XP_011508872.1:n.4216+13928C=
XM_011510572.3:c.3033C= XP_011508874.1:p.Cys1011=
XM_017003296.1:c.4707C= XP_016858785.1:p.Cys1569=
XM_017003297.1:c.4590C= XP_016858786.1:p.Cys1530=
XM_017003298.1:c.4707C= XP_016858787.1:p.Cys1569=
XM_017003300.1:c.4216+13928C= XP_016858789.1:n.4216+13928C=
XR_001738602.1:n.5033C=
XR_001738603.1:n.5033C=
XR_001738604.1:n.4779C=
XR_001738606.1:n.4542+13928C=
XR_001738607.1:n.4542+13928C=
XR_922837.2:n.5033C=
NM_000092.5:c.4707C= MANE Select NP_000083.3:p.Cys1569=