Canonical Allele Identifier: CA2450718783

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108686110A= , CM000685.2:g.108686110A=	GRCh38
NC_000023.10:g.107929340A= , CM000685.1:g.107929340A=	GRCh37
NC_000023.9:g.107815996A=	NCBI36
NG_011977.1:g.251187A=
NG_011977.2:g.251187A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4296A= MANE Select	ENSP00000331902.7:p.Pro1432=
ENST00000361603.7:c.4278A=	ENSP00000354505.2:p.Pro1426=
ENST00000510690.2:n.790A=
ENST00000328300.10:c.4296A=	ENSP00000331902.6:p.Pro1432=
ENST00000361603.6:c.4278A=	ENSP00000354505.2:p.Pro1426=
ENST00000489230.1:n.699A=
ENST00000515658.1:c.92A=
NM_000495.4:c.4278A=	NP_000486.1:p.Pro1426=
NM_033380.2:c.4296A=	NP_203699.1:p.Pro1432=
XM_005262070.2:c.4287A=	XP_005262127.1:p.Pro1429=
XM_006724616.2:c.4296A=	XP_006724679.1:p.Pro1432=
XM_011530849.1:c.3972A=	XP_011529151.1:p.Pro1324=
XM_011530851.1:c.1869A=	XP_011529153.1:p.Pro623=
XM_011530849.2:c.4311A=	XP_011529151.2:p.Pro1437=
XM_017029259.2:c.4302A=	XP_016884748.1:p.Pro1434=
XM_017029260.1:c.4293A=	XP_016884749.1:p.Pro1431=
XM_017029263.2:c.2631A=	XP_016884752.1:p.Pro877=
NM_000495.5:c.4278A=	NP_000486.1:p.Pro1426=
NM_033380.3:c.4296A= MANE Select	NP_203699.1:p.Pro1432=