Canonical Allele Identifier: CA2450719216

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687505C= , CM000685.2:g.108687505C=	GRCh38
NC_000023.10:g.107930735C= , CM000685.1:g.107930735C=	GRCh37
NC_000023.9:g.107817391C=	NCBI36
NG_011977.1:g.252582C=
NG_011977.2:g.252582C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4339C= MANE Select	ENSP00000331902.7:p.Pro1447=
ENST00000361603.7:c.4321C=	ENSP00000354505.2:p.Pro1441=
ENST00000510690.2:n.833C=
ENST00000328300.10:c.4339C=	ENSP00000331902.6:p.Pro1447=
ENST00000361603.6:c.4321C=	ENSP00000354505.2:p.Pro1441=
ENST00000515658.1:c.135C=
NM_000495.4:c.4321C=	NP_000486.1:p.Pro1441=
NM_033380.2:c.4339C=	NP_203699.1:p.Pro1447=
XM_005262070.2:c.4330C=	XP_005262127.1:p.Pro1444=
XM_006724616.2:c.4339C=	XP_006724679.1:p.Pro1447=
XM_011530849.1:c.4015C=	XP_011529151.1:p.Pro1339=
XM_011530851.1:c.1912C=	XP_011529153.1:p.Pro638=
XM_011530849.2:c.4354C=	XP_011529151.2:p.Pro1452=
XM_017029259.2:c.4345C=	XP_016884748.1:p.Pro1449=
XM_017029260.1:c.4336C=	XP_016884749.1:p.Pro1446=
XM_017029263.2:c.2674C=	XP_016884752.1:p.Pro892=
NM_000495.5:c.4321C=	NP_000486.1:p.Pro1441=
NM_033380.3:c.4339C= MANE Select	NP_203699.1:p.Pro1447=