Canonical Allele Identifier: CA2754500292

Gene: COL4A4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227008342_227008343insA , CM000664.2:g.227008342_227008343insA	GRCh38
NC_000002.11:g.227873058_227873059insA , CM000664.1:g.227873058_227873059insA	GRCh37
NC_000002.10:g.227581302_227581303insA	NCBI36
NG_011592.1:g.161217_161218insT , LRG_231:g.161217_161218insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682098.1:c.190-104_190-103insT	ENSP00000508331.1:n.190-104_190-103insT
ENST00000396625.5:c.4523-39_4523-38insT MANE Select	ENSP00000379866.3:n.4523-39_4523-38insT
ENST00000396625.3:c.4523-39_4523-38insT	ENSP00000379866.3:n.4523-39_4523-38insT
NM_000092.4:c.4523-39_4523-38insT , LRG_231t1:c.4523-39_4523-38insT	NP_000083.3:n.4523-39_4523-38insT
XM_005246281.2:c.4523-39_4523-38insT	XP_005246338.1:n.4523-39_4523-38insT
XM_005246282.2:c.3968-39_3968-38insT	XP_005246339.1:n.3968-39_3968-38insT
XM_006712246.2:c.4334-39_4334-38insT	XP_006712309.1:n.4334-39_4334-38insT
XM_006712249.2:c.4523-39_4523-38insT	XP_006712312.1:n.4523-39_4523-38insT
XM_006712252.2:c.4216+13705_4216+13706insT	XP_006712315.1:n.4216+13705_4216+13706insT
XM_011510557.1:c.4442-39_4442-38insT	XP_011508859.1:n.4442-39_4442-38insT
XM_011510558.1:c.4415-39_4415-38insT	XP_011508860.1:n.4415-39_4415-38insT
XM_011510559.1:c.4523-39_4523-38insT	XP_011508861.1:n.4523-39_4523-38insT
XM_011510560.1:c.4523-39_4523-38insT	XP_011508862.1:n.4523-39_4523-38insT
XM_011510561.1:c.4523-39_4523-38insT	XP_011508863.1:n.4523-39_4523-38insT
XM_011510562.1:c.4523-39_4523-38insT	XP_011508864.1:n.4523-39_4523-38insT
XM_011510563.1:c.4334-104_4334-103insT	XP_011508865.1:n.4334-104_4334-103insT
XM_011510564.1:c.4217-104_4217-103insT	XP_011508866.1:n.4217-104_4217-103insT
XM_011510565.1:c.4216+13705_4216+13706insT	XP_011508867.1:n.4216+13705_4216+13706insT
XM_011510566.1:c.4216+13705_4216+13706insT	XP_011508868.1:n.4216+13705_4216+13706insT
XM_011510567.1:c.4216+13705_4216+13706insT	XP_011508869.1:n.4216+13705_4216+13706insT
XM_011510569.1:c.4216+13705_4216+13706insT	XP_011508871.1:n.4216+13705_4216+13706insT
XM_011510570.1:c.4216+13705_4216+13706insT	XP_011508872.1:n.4216+13705_4216+13706insT
XM_011510571.1:c.4216+13705_4216+13706insT	XP_011508873.1:n.4216+13705_4216+13706insT
XM_011510572.1:c.2849-39_2849-38insT	XP_011508874.1:n.2849-39_2849-38insT
XR_922837.1:n.4833-39_4833-38insT
XR_922838.1:n.4833-39_4833-38insT
XR_922839.1:n.4526+13705_4526+13706insT
XR_922840.1:n.4526+13705_4526+13706insT
XM_005246281.3:c.4523-39_4523-38insT	XP_005246338.1:n.4523-39_4523-38insT
XM_005246282.3:c.3968-39_3968-38insT	XP_005246339.1:n.3968-39_3968-38insT
XM_006712246.3:c.4334-39_4334-38insT	XP_006712309.1:n.4334-39_4334-38insT
XM_011510557.2:c.4442-39_4442-38insT	XP_011508859.1:n.4442-39_4442-38insT
XM_011510558.2:c.4415-39_4415-38insT	XP_011508860.1:n.4415-39_4415-38insT
XM_011510559.2:c.4523-39_4523-38insT	XP_011508861.1:n.4523-39_4523-38insT
XM_011510560.2:c.4523-39_4523-38insT	XP_011508862.1:n.4523-39_4523-38insT
XM_011510561.2:c.4523-39_4523-38insT	XP_011508863.1:n.4523-39_4523-38insT
XM_011510562.2:c.4523-39_4523-38insT	XP_011508864.1:n.4523-39_4523-38insT
XM_011510565.2:c.4216+13705_4216+13706insT	XP_011508867.1:n.4216+13705_4216+13706insT
XM_011510566.2:c.4216+13705_4216+13706insT	XP_011508868.1:n.4216+13705_4216+13706insT
XM_011510567.2:c.4216+13705_4216+13706insT	XP_011508869.1:n.4216+13705_4216+13706insT
XM_011510569.2:c.4216+13705_4216+13706insT	XP_011508871.1:n.4216+13705_4216+13706insT
XM_011510570.2:c.4216+13705_4216+13706insT	XP_011508872.1:n.4216+13705_4216+13706insT
XM_011510572.3:c.2849-39_2849-38insT	XP_011508874.1:n.2849-39_2849-38insT
XM_017003296.1:c.4523-39_4523-38insT	XP_016858785.1:n.4523-39_4523-38insT
XM_017003297.1:c.4406-39_4406-38insT	XP_016858786.1:n.4406-39_4406-38insT
XM_017003298.1:c.4523-39_4523-38insT	XP_016858787.1:n.4523-39_4523-38insT
XM_017003300.1:c.4216+13705_4216+13706insT	XP_016858789.1:n.4216+13705_4216+13706insT
XR_001738602.1:n.4849-39_4849-38insT
XR_001738603.1:n.4849-39_4849-38insT
XR_001738604.1:n.4660-104_4660-103insT
XR_001738606.1:n.4542+13705_4542+13706insT
XR_001738607.1:n.4542+13705_4542+13706insT
XR_922837.2:n.4849-39_4849-38insT
NM_000092.5:c.4523-39_4523-38insT MANE Select	NP_000083.3:n.4523-39_4523-38insT