Canonical Allele Identifier: CA2450716911

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108680937G= , CM000685.2:g.108680937G=	GRCh38
NC_000023.10:g.107924167G= , CM000685.1:g.107924167G=	GRCh37
NC_000023.9:g.107810823G=	NCBI36
NG_011977.1:g.246014G=
NG_011977.2:g.246014G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4068G= MANE Select	ENSP00000331902.7:p.Pro1356=
ENST00000361603.7:c.4050G=	ENSP00000354505.2:p.Pro1350=
ENST00000510690.2:n.562G=
ENST00000328300.10:c.4068G=	ENSP00000331902.6:p.Pro1356=
ENST00000361603.6:c.4050G=	ENSP00000354505.2:p.Pro1350=
ENST00000489230.1:n.471G=
NM_000495.4:c.4050G=	NP_000486.1:p.Pro1350=
NM_033380.2:c.4068G=	NP_203699.1:p.Pro1356=
XM_005262070.2:c.4059G=	XP_005262127.1:p.Pro1353=
XM_006724616.2:c.4068G=	XP_006724679.1:p.Pro1356=
XM_011530849.1:c.3744G=	XP_011529151.1:p.Pro1248=
XM_011530851.1:c.1641G=	XP_011529153.1:p.Pro547=
XM_011530849.2:c.4083G=	XP_011529151.2:p.Pro1361=
XM_017029259.2:c.4074G=	XP_016884748.1:p.Pro1358=
XM_017029260.1:c.4065G=	XP_016884749.1:p.Pro1355=
XM_017029263.2:c.2403G=	XP_016884752.1:p.Pro801=
NM_000495.5:c.4050G=	NP_000486.1:p.Pro1350=
NM_033380.3:c.4068G= MANE Select	NP_203699.1:p.Pro1356=