Canonical Allele Identifier: CA2450721868

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695695T= , CM000685.2:g.108695695T=	GRCh38
NC_000023.10:g.107938925T= , CM000685.1:g.107938925T=	GRCh37
NC_000023.9:g.107825581T=	NCBI36
NG_011977.1:g.260772T=
NG_011977.2:g.260772T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4994+256T= MANE Select	ENSP00000331902.7:n.4994+256T=
ENST00000361603.7:c.4976+256T=	ENSP00000354505.2:n.4976+256T=
ENST00000510690.2:n.1488+256T=
ENST00000644079.1:n.2081T=
ENST00000328300.10:c.4994+256T=	ENSP00000331902.6:n.4994+256T=
ENST00000361603.6:c.4976+256T=	ENSP00000354505.2:n.4976+256T=
ENST00000504541.1:c.220-602T=	ENSP00000424845.1:n.220-602T=
ENST00000515658.1:c.325-602T=
NM_000495.4:c.4976+256T=	NP_000486.1:n.4976+256T=
NM_033380.2:c.4994+256T=	NP_203699.1:n.4994+256T=
XM_005262070.2:c.4985+256T=	XP_005262127.1:n.4985+256T=
XM_006724616.2:c.4994+256T=	XP_006724679.1:n.4994+256T=
XM_011530849.1:c.4670+256T=	XP_011529151.1:n.4670+256T=
XM_011530851.1:c.2567+256T=	XP_011529153.1:n.2567+256T=
XM_011530849.2:c.5009+256T=	XP_011529151.2:n.5009+256T=
XM_017029259.2:c.5000+256T=	XP_016884748.1:n.5000+256T=
XM_017029260.1:c.4991+256T=	XP_016884749.1:n.4991+256T=
XM_017029263.2:c.3329+256T=	XP_016884752.1:n.3329+256T=
NM_000495.5:c.4976+256T=	NP_000486.1:n.4976+256T=
NM_033380.3:c.4994+256T= MANE Select	NP_203699.1:n.4994+256T=