Canonical Allele Identifier: CA2450716901

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108680893G= , CM000685.2:g.108680893G=	GRCh38
NC_000023.10:g.107924123G= , CM000685.1:g.107924123G=	GRCh37
NC_000023.9:g.107810779G=	NCBI36
NG_011977.1:g.245970G=
NG_011977.2:g.245970G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4024G= MANE Select	ENSP00000331902.7:p.Gly1342=
ENST00000361603.7:c.4006G=	ENSP00000354505.2:p.Gly1336=
ENST00000510690.2:n.518G=
ENST00000328300.10:c.4024G=	ENSP00000331902.6:p.Gly1342=
ENST00000361603.6:c.4006G=	ENSP00000354505.2:p.Gly1336=
ENST00000489230.1:n.427G=
NM_000495.4:c.4006G=	NP_000486.1:p.Gly1336=
NM_033380.2:c.4024G=	NP_203699.1:p.Gly1342=
XM_005262070.2:c.4015G=	XP_005262127.1:p.Gly1339=
XM_006724616.2:c.4024G=	XP_006724679.1:p.Gly1342=
XM_011530849.1:c.3700G=	XP_011529151.1:p.Gly1234=
XM_011530851.1:c.1597G=	XP_011529153.1:p.Gly533=
XM_011530849.2:c.4039G=	XP_011529151.2:p.Gly1347=
XM_017029259.2:c.4030G=	XP_016884748.1:p.Gly1344=
XM_017029260.1:c.4021G=	XP_016884749.1:p.Gly1341=
XM_017029263.2:c.2359G=	XP_016884752.1:p.Gly787=
NM_000495.5:c.4006G=	NP_000486.1:p.Gly1336=
NM_033380.3:c.4024G= MANE Select	NP_203699.1:p.Gly1342=