Canonical Allele Identifier: CA2450721914

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695827G= , CM000685.2:g.108695827G=	GRCh38
NC_000023.10:g.107939057G= , CM000685.1:g.107939057G=	GRCh37
NC_000023.9:g.107825713G=	NCBI36
NG_011977.1:g.260904G=
NG_011977.2:g.260904G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4994+388G= MANE Select	ENSP00000331902.7:n.4994+388G=
ENST00000361603.7:c.4976+388G=	ENSP00000354505.2:n.4976+388G=
ENST00000510690.2:n.1488+388G=
ENST00000644079.1:n.2213G=
ENST00000328300.10:c.4994+388G=	ENSP00000331902.6:n.4994+388G=
ENST00000361603.6:c.4976+388G=	ENSP00000354505.2:n.4976+388G=
ENST00000504541.1:c.220-470G=	ENSP00000424845.1:n.220-470G=
ENST00000515658.1:c.325-470G=
NM_000495.4:c.4976+388G=	NP_000486.1:n.4976+388G=
NM_033380.2:c.4994+388G=	NP_203699.1:n.4994+388G=
XM_005262070.2:c.4985+388G=	XP_005262127.1:n.4985+388G=
XM_006724616.2:c.4994+388G=	XP_006724679.1:n.4994+388G=
XM_011530849.1:c.4670+388G=	XP_011529151.1:n.4670+388G=
XM_011530851.1:c.2567+388G=	XP_011529153.1:n.2567+388G=
XM_011530849.2:c.5009+388G=	XP_011529151.2:n.5009+388G=
XM_017029259.2:c.5000+388G=	XP_016884748.1:n.5000+388G=
XM_017029260.1:c.4991+388G=	XP_016884749.1:n.4991+388G=
XM_017029263.2:c.3329+388G=	XP_016884752.1:n.3329+388G=
NM_000495.5:c.4976+388G=	NP_000486.1:n.4976+388G=
NM_033380.3:c.4994+388G= MANE Select	NP_203699.1:n.4994+388G=