Canonical Allele Identifier: CA2450722140

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108696516T= , CM000685.2:g.108696516T=	GRCh38
NC_000023.10:g.107939746T= , CM000685.1:g.107939746T=	GRCh37
NC_000023.9:g.107826402T=	NCBI36
NG_011977.1:g.261593T=
NG_011977.2:g.261593T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.*138T= MANE Select	ENSP00000331902.7:n.*138T=
ENST00000361603.7:c.*138T=	ENSP00000354505.2:n.*138T=
ENST00000644079.1:n.2902T=
ENST00000328300.10:c.*138T=	ENSP00000331902.6:n.*138T=
ENST00000361603.6:c.*138T=	ENSP00000354505.2:n.*138T=
ENST00000504541.1:c.439T=	ENSP00000424845.1:n.439T=
ENST00000515658.1:c.544T=
NM_000495.4:c.*138T=	NP_000486.1:n.*138T=
NM_033380.2:c.*138T=	NP_203699.1:n.*138T=
XM_005262070.2:c.*138T=	XP_005262127.1:n.*138T=
XM_006724616.2:c.*138T=	XP_006724679.1:n.*138T=
XM_011530849.1:c.*138T=	XP_011529151.1:n.*138T=
XM_011530851.1:c.*138T=	XP_011529153.1:n.*138T=
XM_011530849.2:c.*138T=	XP_011529151.2:n.*138T=
XM_017029259.2:c.*138T=	XP_016884748.1:n.*138T=
XM_017029260.1:c.*138T=	XP_016884749.1:n.*138T=
XM_017029263.2:c.*138T=	XP_016884752.1:n.*138T=
NM_000495.5:c.*138T=	NP_000486.1:n.*138T=
NM_033380.3:c.*138T= MANE Select	NP_203699.1:n.*138T=