Canonical Allele Identifier: CA1332724002

Gene: COL4A4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227008291A= , CM000664.2:g.227008291A=	GRCh38
NC_000002.11:g.227873007A= , CM000664.1:g.227873007A=	GRCh37
NC_000002.10:g.227581251A=	NCBI36
NG_011592.1:g.161269T= , LRG_231:g.161269T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682098.1:c.190-52T=	ENSP00000508331.1:n.190-52T=
ENST00000396625.5:c.4536T= MANE Select	ENSP00000379866.3:p.Ser1512=
ENST00000396625.3:c.4536T=	ENSP00000379866.3:p.Ser1512=
NM_000092.4:c.4536T= , LRG_231t1:c.4536T=	NP_000083.3:p.Ser1512=
XM_005246281.2:c.4536T=	XP_005246338.1:p.Ser1512=
XM_005246282.2:c.3981T=	XP_005246339.1:p.Ser1327=
XM_006712246.2:c.4347T=	XP_006712309.1:p.Ser1449=
XM_006712249.2:c.4536T=	XP_006712312.1:p.Ser1512=
XM_006712252.2:c.4216+13757T=	XP_006712315.1:n.4216+13757T=
XM_011510557.1:c.4455T=	XP_011508859.1:p.Ser1485=
XM_011510558.1:c.4428T=	XP_011508860.1:p.Ser1476=
XM_011510559.1:c.4536T=	XP_011508861.1:p.Ser1512=
XM_011510560.1:c.4536T=	XP_011508862.1:p.Ser1512=
XM_011510561.1:c.4536T=	XP_011508863.1:p.Ser1512=
XM_011510562.1:c.4536T=	XP_011508864.1:p.Ser1512=
XM_011510563.1:c.4334-52T=	XP_011508865.1:n.4334-52T=
XM_011510564.1:c.4217-52T=	XP_011508866.1:n.4217-52T=
XM_011510565.1:c.4216+13757T=	XP_011508867.1:n.4216+13757T=
XM_011510566.1:c.4216+13757T=	XP_011508868.1:n.4216+13757T=
XM_011510567.1:c.4216+13757T=	XP_011508869.1:n.4216+13757T=
XM_011510569.1:c.4216+13757T=	XP_011508871.1:n.4216+13757T=
XM_011510570.1:c.4216+13757T=	XP_011508872.1:n.4216+13757T=
XM_011510571.1:c.4216+13757T=	XP_011508873.1:n.4216+13757T=
XM_011510572.1:c.2862T=	XP_011508874.1:p.Ser954=
XR_922837.1:n.4846T=
XR_922838.1:n.4846T=
XR_922839.1:n.4526+13757T=
XR_922840.1:n.4526+13757T=
XM_005246281.3:c.4536T=	XP_005246338.1:p.Ser1512=
XM_005246282.3:c.3981T=	XP_005246339.1:p.Ser1327=
XM_006712246.3:c.4347T=	XP_006712309.1:p.Ser1449=
XM_011510557.2:c.4455T=	XP_011508859.1:p.Ser1485=
XM_011510558.2:c.4428T=	XP_011508860.1:p.Ser1476=
XM_011510559.2:c.4536T=	XP_011508861.1:p.Ser1512=
XM_011510560.2:c.4536T=	XP_011508862.1:p.Ser1512=
XM_011510561.2:c.4536T=	XP_011508863.1:p.Ser1512=
XM_011510562.2:c.4536T=	XP_011508864.1:p.Ser1512=
XM_011510565.2:c.4216+13757T=	XP_011508867.1:n.4216+13757T=
XM_011510566.2:c.4216+13757T=	XP_011508868.1:n.4216+13757T=
XM_011510567.2:c.4216+13757T=	XP_011508869.1:n.4216+13757T=
XM_011510569.2:c.4216+13757T=	XP_011508871.1:n.4216+13757T=
XM_011510570.2:c.4216+13757T=	XP_011508872.1:n.4216+13757T=
XM_011510572.3:c.2862T=	XP_011508874.1:p.Ser954=
XM_017003296.1:c.4536T=	XP_016858785.1:p.Ser1512=
XM_017003297.1:c.4419T=	XP_016858786.1:p.Ser1473=
XM_017003298.1:c.4536T=	XP_016858787.1:p.Ser1512=
XM_017003300.1:c.4216+13757T=	XP_016858789.1:n.4216+13757T=
XR_001738602.1:n.4862T=
XR_001738603.1:n.4862T=
XR_001738604.1:n.4660-52T=
XR_001738606.1:n.4542+13757T=
XR_001738607.1:n.4542+13757T=
XR_922837.2:n.4862T=
NM_000092.5:c.4536T= MANE Select	NP_000083.3:p.Ser1512=