Canonical Allele Identifier: CA2450721723

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695273A= , CM000685.2:g.108695273A=	GRCh38
NC_000023.10:g.107938503A= , CM000685.1:g.107938503A=	GRCh37
NC_000023.9:g.107825159A=	NCBI36
NG_011977.1:g.260350A=
NG_011977.2:g.260350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4828A= MANE Select	ENSP00000331902.7:p.Ser1610=
ENST00000361603.7:c.4810A=	ENSP00000354505.2:p.Ser1604=
ENST00000510690.2:n.1322A=
ENST00000644079.1:n.1659A=
ENST00000328300.10:c.4828A=	ENSP00000331902.6:p.Ser1610=
ENST00000361603.6:c.4810A=	ENSP00000354505.2:p.Ser1604=
ENST00000504541.1:c.219+352A=	ENSP00000424845.1:n.219+352A=
ENST00000515658.1:c.325-1024A=
NM_000495.4:c.4810A=	NP_000486.1:p.Ser1604=
NM_033380.2:c.4828A=	NP_203699.1:p.Ser1610=
XM_005262070.2:c.4819A=	XP_005262127.1:p.Ser1607=
XM_006724616.2:c.4828A=	XP_006724679.1:p.Ser1610=
XM_011530849.1:c.4504A=	XP_011529151.1:p.Ser1502=
XM_011530851.1:c.2401A=	XP_011529153.1:p.Ser801=
XM_011530849.2:c.4843A=	XP_011529151.2:p.Ser1615=
XM_017029259.2:c.4834A=	XP_016884748.1:p.Ser1612=
XM_017029260.1:c.4825A=	XP_016884749.1:p.Ser1609=
XM_017029263.2:c.3163A=	XP_016884752.1:p.Ser1055=
NM_000495.5:c.4810A=	NP_000486.1:p.Ser1604=
NM_033380.3:c.4828A= MANE Select	NP_203699.1:p.Ser1610=