Canonical Allele Identifier: CA2450722062

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108696301C= , CM000685.2:g.108696301C=	GRCh38
NC_000023.10:g.107939531C= , CM000685.1:g.107939531C=	GRCh37
NC_000023.9:g.107826187C=	NCBI36
NG_011977.1:g.261378C=
NG_011977.2:g.261378C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4999C= MANE Select	ENSP00000331902.7:p.Pro1667=
ENST00000361603.7:c.4981C=	ENSP00000354505.2:p.Pro1661=
ENST00000510690.2:n.1493C=
ENST00000644079.1:n.2687C=
ENST00000328300.10:c.4999C=	ENSP00000331902.6:p.Pro1667=
ENST00000361603.6:c.4981C=	ENSP00000354505.2:p.Pro1661=
ENST00000504541.1:c.224C=	ENSP00000424845.1:n.224C=
ENST00000515658.1:c.329C=
NM_000495.4:c.4981C=	NP_000486.1:p.Pro1661=
NM_033380.2:c.4999C=	NP_203699.1:p.Pro1667=
XM_005262070.2:c.4990C=	XP_005262127.1:p.Pro1664=
XM_006724616.2:c.4999C=	XP_006724679.1:p.Pro1667=
XM_011530849.1:c.4675C=	XP_011529151.1:p.Pro1559=
XM_011530851.1:c.2572C=	XP_011529153.1:p.Pro858=
XM_011530849.2:c.5014C=	XP_011529151.2:p.Pro1672=
XM_017029259.2:c.5005C=	XP_016884748.1:p.Pro1669=
XM_017029260.1:c.4996C=	XP_016884749.1:p.Pro1666=
XM_017029263.2:c.3334C=	XP_016884752.1:p.Pro1112=
NM_000495.5:c.4981C=	NP_000486.1:p.Pro1661=
NM_033380.3:c.4999C= MANE Select	NP_203699.1:p.Pro1667=