Canonical Allele Identifier: CA2450718801

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108686171T= , CM000685.2:g.108686171T=	GRCh38
NC_000023.10:g.107929401T= , CM000685.1:g.107929401T=	GRCh37
NC_000023.9:g.107816057T=	NCBI36
NG_011977.1:g.251248T=
NG_011977.2:g.251248T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4315+42T= MANE Select	ENSP00000331902.7:n.4315+42T=
ENST00000361603.7:c.4297+42T=	ENSP00000354505.2:n.4297+42T=
ENST00000510690.2:n.809+42T=
ENST00000328300.10:c.4315+42T=	ENSP00000331902.6:n.4315+42T=
ENST00000361603.6:c.4297+42T=	ENSP00000354505.2:n.4297+42T=
ENST00000489230.1:n.718+42T=
ENST00000515658.1:c.111+42T=
NM_000495.4:c.4297+42T=	NP_000486.1:n.4297+42T=
NM_033380.2:c.4315+42T=	NP_203699.1:n.4315+42T=
XM_005262070.2:c.4306+42T=	XP_005262127.1:n.4306+42T=
XM_006724616.2:c.4315+42T=	XP_006724679.1:n.4315+42T=
XM_011530849.1:c.3991+42T=	XP_011529151.1:n.3991+42T=
XM_011530851.1:c.1888+42T=	XP_011529153.1:n.1888+42T=
XM_011530849.2:c.4330+42T=	XP_011529151.2:n.4330+42T=
XM_017029259.2:c.4321+42T=	XP_016884748.1:n.4321+42T=
XM_017029260.1:c.4312+42T=	XP_016884749.1:n.4312+42T=
XM_017029263.2:c.2650+42T=	XP_016884752.1:n.2650+42T=
NM_000495.5:c.4297+42T=	NP_000486.1:n.4297+42T=
NM_033380.3:c.4315+42T= MANE Select	NP_203699.1:n.4315+42T=