Canonical Allele Identifier: CA1332734862
Gene: COL4A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227032261C= , CM000664.2:g.227032261C= GRCh38
NC_000002.11:g.227896977C= , CM000664.1:g.227896977C= GRCh37
NC_000002.10:g.227605221C= NCBI36
NG_011592.1:g.137299G= , LRG_231:g.137299G=

Transcript Alleles

HGVS Amino-acid change
ENST00000396625.5:c.3593G= MANE Select ENSP00000379866.3:p.Gly1198=
ENST00000396625.3:c.3593G= ENSP00000379866.3:p.Gly1198=
NM_000092.4:c.3593G= , LRG_231t1:c.3593G= NP_000083.3:p.Gly1198=
XM_005246281.2:c.3593G= XP_005246338.1:p.Gly1198=
XM_005246282.2:c.3038G= XP_005246339.1:p.Gly1013=
XM_006712246.2:c.3593G= XP_006712309.1:p.Gly1198=
XM_006712249.2:c.3593G= XP_006712312.1:p.Gly1198=
XM_006712251.2:c.3593G= XP_006712314.1:p.Gly1198=
XM_006712252.2:c.3593G= XP_006712315.1:p.Gly1198=
XM_011510557.1:c.3512G= XP_011508859.1:p.Gly1171=
XM_011510558.1:c.3485G= XP_011508860.1:p.Gly1162=
XM_011510559.1:c.3593G= XP_011508861.1:p.Gly1198=
XM_011510560.1:c.3593G= XP_011508862.1:p.Gly1198=
XM_011510561.1:c.3593G= XP_011508863.1:p.Gly1198=
XM_011510562.1:c.3593G= XP_011508864.1:p.Gly1198=
XM_011510563.1:c.3593G= XP_011508865.1:p.Gly1198=
XM_011510564.1:c.3593G= XP_011508866.1:p.Gly1198=
XM_011510565.1:c.3593G= XP_011508867.1:p.Gly1198=
XM_011510566.1:c.3593G= XP_011508868.1:p.Gly1198=
XM_011510567.1:c.3593G= XP_011508869.1:p.Gly1198=
XM_011510568.1:c.3593G= XP_011508870.1:p.Gly1198=
XM_011510569.1:c.3593G= XP_011508871.1:p.Gly1198=
XM_011510570.1:c.3593G= XP_011508872.1:p.Gly1198=
XM_011510571.1:c.3593G= XP_011508873.1:p.Gly1198=
XM_011510572.1:c.1919G= XP_011508874.1:p.Gly640=
XR_922837.1:n.3903G=
XR_922838.1:n.3903G=
XR_922839.1:n.3903G=
XR_922840.1:n.3903G=
XM_005246281.3:c.3593G= XP_005246338.1:p.Gly1198=
XM_005246282.3:c.3038G= XP_005246339.1:p.Gly1013=
XM_006712246.3:c.3593G= XP_006712309.1:p.Gly1198=
XM_011510557.2:c.3512G= XP_011508859.1:p.Gly1171=
XM_011510558.2:c.3485G= XP_011508860.1:p.Gly1162=
XM_011510559.2:c.3593G= XP_011508861.1:p.Gly1198=
XM_011510560.2:c.3593G= XP_011508862.1:p.Gly1198=
XM_011510561.2:c.3593G= XP_011508863.1:p.Gly1198=
XM_011510562.2:c.3593G= XP_011508864.1:p.Gly1198=
XM_011510565.2:c.3593G= XP_011508867.1:p.Gly1198=
XM_011510566.2:c.3593G= XP_011508868.1:p.Gly1198=
XM_011510567.2:c.3593G= XP_011508869.1:p.Gly1198=
XM_011510568.2:c.3593G= XP_011508870.1:p.Gly1198=
XM_011510569.2:c.3593G= XP_011508871.1:p.Gly1198=
XM_011510570.2:c.3593G= XP_011508872.1:p.Gly1198=
XM_011510572.3:c.1919G= XP_011508874.1:p.Gly640=
XM_017003296.1:c.3593G= XP_016858785.1:p.Gly1198=
XM_017003297.1:c.3476G= XP_016858786.1:p.Gly1159=
XM_017003298.1:c.3593G= XP_016858787.1:p.Gly1198=
XM_017003299.1:c.3593G= XP_016858788.1:p.Gly1198=
XM_017003300.1:c.3593G= XP_016858789.1:p.Gly1198=
XR_001738602.1:n.3919G=
XR_001738603.1:n.3919G=
XR_001738604.1:n.3919G=
XR_001738606.1:n.3919G=
XR_001738607.1:n.3919G=
XR_922837.2:n.3919G=
NM_000092.5:c.3593G= MANE Select NP_000083.3:p.Gly1198=