Canonical Allele Identifier: CA2450719239

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687671A= , CM000685.2:g.108687671A=	GRCh38
NC_000023.10:g.107930901A= , CM000685.1:g.107930901A=	GRCh37
NC_000023.9:g.107817557A=	NCBI36
NG_011977.1:g.252748A=
NG_011977.2:g.252748A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4505A= MANE Select	ENSP00000331902.7:p.Lys1502=
ENST00000361603.7:c.4487A=	ENSP00000354505.2:p.Lys1496=
ENST00000510690.2:n.999A=
ENST00000328300.10:c.4505A=	ENSP00000331902.6:p.Lys1502=
ENST00000361603.6:c.4487A=	ENSP00000354505.2:p.Lys1496=
ENST00000515658.1:c.301A=
NM_000495.4:c.4487A=	NP_000486.1:p.Lys1496=
NM_033380.2:c.4505A=	NP_203699.1:p.Lys1502=
XM_005262070.2:c.4496A=	XP_005262127.1:p.Lys1499=
XM_006724616.2:c.4505A=	XP_006724679.1:p.Lys1502=
XM_011530849.1:c.4181A=	XP_011529151.1:p.Lys1394=
XM_011530851.1:c.2078A=	XP_011529153.1:p.Lys693=
XM_011530849.2:c.4520A=	XP_011529151.2:p.Lys1507=
XM_017029259.2:c.4511A=	XP_016884748.1:p.Lys1504=
XM_017029260.1:c.4502A=	XP_016884749.1:p.Lys1501=
XM_017029263.2:c.2840A=	XP_016884752.1:p.Lys947=
NM_000495.5:c.4487A=	NP_000486.1:p.Lys1496=
NM_033380.3:c.4505A= MANE Select	NP_203699.1:p.Lys1502=