Canonical Allele Identifier: CA1332730220
Gene: COL4A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227021983_227021984delinsAG , CM000664.2:g.227021983_227021984delinsAG GRCh38
NC_000002.11:g.227886699_227886700delinsAG , CM000664.1:g.227886699_227886700delinsAG GRCh37
NC_000002.10:g.227594943_227594944delinsAG NCBI36
NG_011592.1:g.147576_147577delinsCT , LRG_231:g.147576_147577delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000396625.5:c.4216+64_4216+65delinsCT MANE Select ENSP00000379866.3:n.4216+64_4216+65delins...
ENST00000396625.3:c.4216+64_4216+65delinsCT ENSP00000379866.3:n.4216+64_4216+65delins...
NM_000092.4:c.4216+64_4216+65delinsCT , LRG_231t1:c.4216+64_4216+65delinsCT NP_000083.3:n.4216+64_4216+65delinsCT
XM_005246281.2:c.4216+64_4216+65delinsCT XP_005246338.1:n.4216+64_4216+65delinsCT
XM_005246282.2:c.3661+64_3661+65delinsCT XP_005246339.1:n.3661+64_3661+65delinsCT
XM_006712246.2:c.4216+64_4216+65delinsCT XP_006712309.1:n.4216+64_4216+65delinsCT
XM_006712249.2:c.4216+64_4216+65delinsCT XP_006712312.1:n.4216+64_4216+65delinsCT
XM_006712251.2:c.4216+64_4216+65delinsCT XP_006712314.1:n.4216+64_4216+65delinsCT
XM_006712252.2:c.4216+64_4216+65delinsCT XP_006712315.1:n.4216+64_4216+65delinsCT
XM_011510557.1:c.4135+64_4135+65delinsCT XP_011508859.1:n.4135+64_4135+65delinsCT
XM_011510558.1:c.4108+64_4108+65delinsCT XP_011508860.1:n.4108+64_4108+65delinsCT
XM_011510559.1:c.4216+64_4216+65delinsCT XP_011508861.1:n.4216+64_4216+65delinsCT
XM_011510560.1:c.4216+64_4216+65delinsCT XP_011508862.1:n.4216+64_4216+65delinsCT
XM_011510561.1:c.4216+64_4216+65delinsCT XP_011508863.1:n.4216+64_4216+65delinsCT
XM_011510562.1:c.4216+64_4216+65delinsCT XP_011508864.1:n.4216+64_4216+65delinsCT
XM_011510563.1:c.4216+64_4216+65delinsCT XP_011508865.1:n.4216+64_4216+65delinsCT
XM_011510564.1:c.4216+64_4216+65delinsCT XP_011508866.1:n.4216+64_4216+65delinsCT
XM_011510565.1:c.4216+64_4216+65delinsCT XP_011508867.1:n.4216+64_4216+65delinsCT
XM_011510566.1:c.4216+64_4216+65delinsCT XP_011508868.1:n.4216+64_4216+65delinsCT
XM_011510567.1:c.4216+64_4216+65delinsCT XP_011508869.1:n.4216+64_4216+65delinsCT
XM_011510568.1:c.4216+64_4216+65delinsCT XP_011508870.1:n.4216+64_4216+65delinsCT
XM_011510569.1:c.4216+64_4216+65delinsCT XP_011508871.1:n.4216+64_4216+65delinsCT
XM_011510570.1:c.4216+64_4216+65delinsCT XP_011508872.1:n.4216+64_4216+65delinsCT
XM_011510571.1:c.4216+64_4216+65delinsCT XP_011508873.1:n.4216+64_4216+65delinsCT
XM_011510572.1:c.2542+64_2542+65delinsCT XP_011508874.1:n.2542+64_2542+65delinsCT
XR_922837.1:n.4526+64_4526+65delinsCT
XR_922838.1:n.4526+64_4526+65delinsCT
XR_922839.1:n.4526+64_4526+65delinsCT
XR_922840.1:n.4526+64_4526+65delinsCT
XM_005246281.3:c.4216+64_4216+65delinsCT XP_005246338.1:n.4216+64_4216+65delinsCT
XM_005246282.3:c.3661+64_3661+65delinsCT XP_005246339.1:n.3661+64_3661+65delinsCT
XM_006712246.3:c.4216+64_4216+65delinsCT XP_006712309.1:n.4216+64_4216+65delinsCT
XM_011510557.2:c.4135+64_4135+65delinsCT XP_011508859.1:n.4135+64_4135+65delinsCT
XM_011510558.2:c.4108+64_4108+65delinsCT XP_011508860.1:n.4108+64_4108+65delinsCT
XM_011510559.2:c.4216+64_4216+65delinsCT XP_011508861.1:n.4216+64_4216+65delinsCT
XM_011510560.2:c.4216+64_4216+65delinsCT XP_011508862.1:n.4216+64_4216+65delinsCT
XM_011510561.2:c.4216+64_4216+65delinsCT XP_011508863.1:n.4216+64_4216+65delinsCT
XM_011510562.2:c.4216+64_4216+65delinsCT XP_011508864.1:n.4216+64_4216+65delinsCT
XM_011510565.2:c.4216+64_4216+65delinsCT XP_011508867.1:n.4216+64_4216+65delinsCT
XM_011510566.2:c.4216+64_4216+65delinsCT XP_011508868.1:n.4216+64_4216+65delinsCT
XM_011510567.2:c.4216+64_4216+65delinsCT XP_011508869.1:n.4216+64_4216+65delinsCT
XM_011510568.2:c.4216+64_4216+65delinsCT XP_011508870.1:n.4216+64_4216+65delinsCT
XM_011510569.2:c.4216+64_4216+65delinsCT XP_011508871.1:n.4216+64_4216+65delinsCT
XM_011510570.2:c.4216+64_4216+65delinsCT XP_011508872.1:n.4216+64_4216+65delinsCT
XM_011510572.3:c.2542+64_2542+65delinsCT XP_011508874.1:n.2542+64_2542+65delinsCT
XM_017003296.1:c.4216+64_4216+65delinsCT XP_016858785.1:n.4216+64_4216+65delinsCT
XM_017003297.1:c.4099+64_4099+65delinsCT XP_016858786.1:n.4099+64_4099+65delinsCT
XM_017003298.1:c.4216+64_4216+65delinsCT XP_016858787.1:n.4216+64_4216+65delinsCT
XM_017003299.1:c.4216+64_4216+65delinsCT XP_016858788.1:n.4216+64_4216+65delinsCT
XM_017003300.1:c.4216+64_4216+65delinsCT XP_016858789.1:n.4216+64_4216+65delinsCT
XR_001738602.1:n.4542+64_4542+65delinsCT
XR_001738603.1:n.4542+64_4542+65delinsCT
XR_001738604.1:n.4542+64_4542+65delinsCT
XR_001738606.1:n.4542+64_4542+65delinsCT
XR_001738607.1:n.4542+64_4542+65delinsCT
XR_922837.2:n.4542+64_4542+65delinsCT
NM_000092.5:c.4216+64_4216+65delinsCT MANE Select NP_000083.3:n.4216+64_4216+65delinsCT