Canonical Allele Identifier: CA1332723970

Gene: COL4A4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227008222_227008224delinsCTG , CM000664.2:g.227008222_227008224delinsCTG	GRCh38
NC_000002.11:g.227872938_227872940delinsCTG , CM000664.1:g.227872938_227872940delinsCTG	GRCh37
NC_000002.10:g.227581182_227581184delinsCTG	NCBI36
NG_011592.1:g.161336_161338delinsCAG , LRG_231:g.161336_161338delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682098.1:c.205_207delinsCAG	ENSP00000508331.1:p.Gln69=
ENST00000396625.5:c.4603_4605delinsCAG MANE Select	ENSP00000379866.3:p.Gln1535=
ENST00000396625.3:c.4603_4605delinsCAG	ENSP00000379866.3:p.Gln1535=
NM_000092.4:c.4603_4605delinsCAG , LRG_231t1:c.4603_4605delinsCAG	NP_000083.3:p.Gln1535=
XM_005246281.2:c.4603_4605delinsCAG	XP_005246338.1:p.Gln1535=
XM_005246282.2:c.4048_4050delinsCAG	XP_005246339.1:p.Gln1350=
XM_006712246.2:c.4414_4416delinsCAG	XP_006712309.1:p.Gln1472=
XM_006712249.2:c.4603_4605delinsCAG	XP_006712312.1:p.Gln1535=
XM_006712252.2:c.4216+13824_4216+13826delinsCAG	XP_006712315.1:n.4216+13824_4216+13826delinsCAG
XM_011510557.1:c.4522_4524delinsCAG	XP_011508859.1:p.Gln1508=
XM_011510558.1:c.4495_4497delinsCAG	XP_011508860.1:p.Gln1499=
XM_011510559.1:c.4603_4605delinsCAG	XP_011508861.1:p.Gln1535=
XM_011510560.1:c.4603_4605delinsCAG	XP_011508862.1:p.Gln1535=
XM_011510561.1:c.4603_4605delinsCAG	XP_011508863.1:p.Gln1535=
XM_011510562.1:c.4603_4605delinsCAG	XP_011508864.1:p.Gln1535=
XM_011510563.1:c.4349_4351delinsCAG	XP_011508865.1:p.Pro1450=
XM_011510564.1:c.4232_4234delinsCAG	XP_011508866.1:p.Pro1411=
XM_011510565.1:c.4216+13824_4216+13826delinsCAG	XP_011508867.1:n.4216+13824_4216+13826delinsCAG
XM_011510566.1:c.4216+13824_4216+13826delinsCAG	XP_011508868.1:n.4216+13824_4216+13826delinsCAG
XM_011510567.1:c.4216+13824_4216+13826delinsCAG	XP_011508869.1:n.4216+13824_4216+13826delinsCAG
XM_011510569.1:c.4216+13824_4216+13826delinsCAG	XP_011508871.1:n.4216+13824_4216+13826delinsCAG
XM_011510570.1:c.4216+13824_4216+13826delinsCAG	XP_011508872.1:n.4216+13824_4216+13826delinsCAG
XM_011510571.1:c.4216+13824_4216+13826delinsCAG	XP_011508873.1:n.4216+13824_4216+13826delinsCAG
XM_011510572.1:c.2929_2931delinsCAG	XP_011508874.1:p.Gln977=
XR_922837.1:n.4913_4915delinsCAG
XR_922838.1:n.4913_4915delinsCAG
XR_922839.1:n.4526+13824_4526+13826delinsCAG
XR_922840.1:n.4526+13824_4526+13826delinsCAG
XM_005246281.3:c.4603_4605delinsCAG	XP_005246338.1:p.Gln1535=
XM_005246282.3:c.4048_4050delinsCAG	XP_005246339.1:p.Gln1350=
XM_006712246.3:c.4414_4416delinsCAG	XP_006712309.1:p.Gln1472=
XM_011510557.2:c.4522_4524delinsCAG	XP_011508859.1:p.Gln1508=
XM_011510558.2:c.4495_4497delinsCAG	XP_011508860.1:p.Gln1499=
XM_011510559.2:c.4603_4605delinsCAG	XP_011508861.1:p.Gln1535=
XM_011510560.2:c.4603_4605delinsCAG	XP_011508862.1:p.Gln1535=
XM_011510561.2:c.4603_4605delinsCAG	XP_011508863.1:p.Gln1535=
XM_011510562.2:c.4603_4605delinsCAG	XP_011508864.1:p.Gln1535=
XM_011510565.2:c.4216+13824_4216+13826delinsCAG	XP_011508867.1:n.4216+13824_4216+13826delinsCAG
XM_011510566.2:c.4216+13824_4216+13826delinsCAG	XP_011508868.1:n.4216+13824_4216+13826delinsCAG
XM_011510567.2:c.4216+13824_4216+13826delinsCAG	XP_011508869.1:n.4216+13824_4216+13826delinsCAG
XM_011510569.2:c.4216+13824_4216+13826delinsCAG	XP_011508871.1:n.4216+13824_4216+13826delinsCAG
XM_011510570.2:c.4216+13824_4216+13826delinsCAG	XP_011508872.1:n.4216+13824_4216+13826delinsCAG
XM_011510572.3:c.2929_2931delinsCAG	XP_011508874.1:p.Gln977=
XM_017003296.1:c.4603_4605delinsCAG	XP_016858785.1:p.Gln1535=
XM_017003297.1:c.4486_4488delinsCAG	XP_016858786.1:p.Gln1496=
XM_017003298.1:c.4603_4605delinsCAG	XP_016858787.1:p.Gln1535=
XM_017003300.1:c.4216+13824_4216+13826delinsCAG	XP_016858789.1:n.4216+13824_4216+13826delinsCAG
XR_001738602.1:n.4929_4931delinsCAG
XR_001738603.1:n.4929_4931delinsCAG
XR_001738604.1:n.4675_4677delinsCAG
XR_001738606.1:n.4542+13824_4542+13826delinsCAG
XR_001738607.1:n.4542+13824_4542+13826delinsCAG
XR_922837.2:n.4929_4931delinsCAG
NM_000092.5:c.4603_4605delinsCAG MANE Select	NP_000083.3:p.Gln1535=