Canonical Allele Identifier: CA2577263055

Gene: COL4A4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227008365_227008369del , CM000664.2:g.227008365_227008369del	GRCh38
NC_000002.11:g.227873081_227873085del , CM000664.1:g.227873081_227873085del	GRCh37
NC_000002.10:g.227581325_227581329del	NCBI36
NG_011592.1:g.161193_161197del , LRG_231:g.161193_161197del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682098.1:c.190-128_190-124del	ENSP00000508331.1:n.190-128_190-124del
ENST00000396625.5:c.4523-63_4523-59del MANE Select	ENSP00000379866.3:n.4523-63_4523-59del
ENST00000396625.3:c.4523-63_4523-59del	ENSP00000379866.3:n.4523-63_4523-59del
NM_000092.4:c.4523-63_4523-59del , LRG_231t1:c.4523-63_4523-59del	NP_000083.3:n.4523-63_4523-59del
XM_005246281.2:c.4523-63_4523-59del	XP_005246338.1:n.4523-63_4523-59del
XM_005246282.2:c.3968-63_3968-59del	XP_005246339.1:n.3968-63_3968-59del
XM_006712246.2:c.4334-63_4334-59del	XP_006712309.1:n.4334-63_4334-59del
XM_006712249.2:c.4523-63_4523-59del	XP_006712312.1:n.4523-63_4523-59del
XM_006712252.2:c.4216+13681_4216+13685del	XP_006712315.1:n.4216+13681_4216+13685del
XM_011510557.1:c.4442-63_4442-59del	XP_011508859.1:n.4442-63_4442-59del
XM_011510558.1:c.4415-63_4415-59del	XP_011508860.1:n.4415-63_4415-59del
XM_011510559.1:c.4523-63_4523-59del	XP_011508861.1:n.4523-63_4523-59del
XM_011510560.1:c.4523-63_4523-59del	XP_011508862.1:n.4523-63_4523-59del
XM_011510561.1:c.4523-63_4523-59del	XP_011508863.1:n.4523-63_4523-59del
XM_011510562.1:c.4523-63_4523-59del	XP_011508864.1:n.4523-63_4523-59del
XM_011510563.1:c.4334-128_4334-124del	XP_011508865.1:n.4334-128_4334-124del
XM_011510564.1:c.4217-128_4217-124del	XP_011508866.1:n.4217-128_4217-124del
XM_011510565.1:c.4216+13681_4216+13685del	XP_011508867.1:n.4216+13681_4216+13685del
XM_011510566.1:c.4216+13681_4216+13685del	XP_011508868.1:n.4216+13681_4216+13685del
XM_011510567.1:c.4216+13681_4216+13685del	XP_011508869.1:n.4216+13681_4216+13685del
XM_011510569.1:c.4216+13681_4216+13685del	XP_011508871.1:n.4216+13681_4216+13685del
XM_011510570.1:c.4216+13681_4216+13685del	XP_011508872.1:n.4216+13681_4216+13685del
XM_011510571.1:c.4216+13681_4216+13685del	XP_011508873.1:n.4216+13681_4216+13685del
XM_011510572.1:c.2849-63_2849-59del	XP_011508874.1:n.2849-63_2849-59del
XR_922837.1:n.4833-63_4833-59del
XR_922838.1:n.4833-63_4833-59del
XR_922839.1:n.4526+13681_4526+13685del
XR_922840.1:n.4526+13681_4526+13685del
XM_005246281.3:c.4523-63_4523-59del	XP_005246338.1:n.4523-63_4523-59del
XM_005246282.3:c.3968-63_3968-59del	XP_005246339.1:n.3968-63_3968-59del
XM_006712246.3:c.4334-63_4334-59del	XP_006712309.1:n.4334-63_4334-59del
XM_011510557.2:c.4442-63_4442-59del	XP_011508859.1:n.4442-63_4442-59del
XM_011510558.2:c.4415-63_4415-59del	XP_011508860.1:n.4415-63_4415-59del
XM_011510559.2:c.4523-63_4523-59del	XP_011508861.1:n.4523-63_4523-59del
XM_011510560.2:c.4523-63_4523-59del	XP_011508862.1:n.4523-63_4523-59del
XM_011510561.2:c.4523-63_4523-59del	XP_011508863.1:n.4523-63_4523-59del
XM_011510562.2:c.4523-63_4523-59del	XP_011508864.1:n.4523-63_4523-59del
XM_011510565.2:c.4216+13681_4216+13685del	XP_011508867.1:n.4216+13681_4216+13685del
XM_011510566.2:c.4216+13681_4216+13685del	XP_011508868.1:n.4216+13681_4216+13685del
XM_011510567.2:c.4216+13681_4216+13685del	XP_011508869.1:n.4216+13681_4216+13685del
XM_011510569.2:c.4216+13681_4216+13685del	XP_011508871.1:n.4216+13681_4216+13685del
XM_011510570.2:c.4216+13681_4216+13685del	XP_011508872.1:n.4216+13681_4216+13685del
XM_011510572.3:c.2849-63_2849-59del	XP_011508874.1:n.2849-63_2849-59del
XM_017003296.1:c.4523-63_4523-59del	XP_016858785.1:n.4523-63_4523-59del
XM_017003297.1:c.4406-63_4406-59del	XP_016858786.1:n.4406-63_4406-59del
XM_017003298.1:c.4523-63_4523-59del	XP_016858787.1:n.4523-63_4523-59del
XM_017003300.1:c.4216+13681_4216+13685del	XP_016858789.1:n.4216+13681_4216+13685del
XR_001738602.1:n.4849-63_4849-59del
XR_001738603.1:n.4849-63_4849-59del
XR_001738604.1:n.4660-128_4660-124del
XR_001738606.1:n.4542+13681_4542+13685del
XR_001738607.1:n.4542+13681_4542+13685del
XR_922837.2:n.4849-63_4849-59del
NM_000092.5:c.4523-63_4523-59del MANE Select	NP_000083.3:n.4523-63_4523-59del