Canonical Allele Identifier: CA2450696017

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108620476A= , CM000685.2:g.108620476A=	GRCh38
NC_000023.10:g.107863706A= , CM000685.1:g.107863706A=	GRCh37
NC_000023.9:g.107750362A=	NCBI36
NG_011977.1:g.185553A=
NG_011977.2:g.185553A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.2677+50A= MANE Select	ENSP00000331902.7:n.2677+50A=
ENST00000361603.7:c.2677+50A=	ENSP00000354505.2:n.2677+50A=
ENST00000328300.10:c.2677+50A=	ENSP00000331902.6:n.2677+50A=
ENST00000361603.6:c.2677+50A=	ENSP00000354505.2:n.2677+50A=
ENST00000483338.1:n.2133+50A=
NM_000495.4:c.2677+50A=	NP_000486.1:n.2677+50A=
NM_033380.2:c.2677+50A=	NP_203699.1:n.2677+50A=
XM_005262070.2:c.2677+50A=	XP_005262127.1:n.2677+50A=
XM_005262072.3:c.2677+50A=	XP_005262129.1:n.2677+50A=
XM_006724616.2:c.2677+50A=	XP_006724679.1:n.2677+50A=
XM_011530849.1:c.2353+50A=	XP_011529151.1:n.2353+50A=
XM_011530850.1:c.2677+50A=	XP_011529152.1:n.2677+50A=
XM_011530851.1:c.250+50A=	XP_011529153.1:n.250+50A=
XM_011530849.2:c.2692+50A=	XP_011529151.2:n.2692+50A=
XM_017029259.2:c.2692+50A=	XP_016884748.1:n.2692+50A=
XM_017029260.1:c.2692+50A=	XP_016884749.1:n.2692+50A=
XM_017029261.1:c.2692+50A=	XP_016884750.1:n.2692+50A=
XM_017029262.2:c.2692+50A=	XP_016884751.1:n.2692+50A=
XM_017029263.2:c.1012+50A=	XP_016884752.1:n.1012+50A=
NM_000495.5:c.2677+50A=	NP_000486.1:n.2677+50A=
NM_033380.3:c.2677+50A= MANE Select	NP_203699.1:n.2677+50A=