Canonical Allele Identifier: CA2450721726

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695278A= , CM000685.2:g.108695278A=	GRCh38
NC_000023.10:g.107938508A= , CM000685.1:g.107938508A=	GRCh37
NC_000023.9:g.107825164A=	NCBI36
NG_011977.1:g.260355A=
NG_011977.2:g.260355A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4833A= MANE Select	ENSP00000331902.7:p.Ala1611=
ENST00000361603.7:c.4815A=	ENSP00000354505.2:p.Ala1605=
ENST00000510690.2:n.1327A=
ENST00000644079.1:n.1664A=
ENST00000328300.10:c.4833A=	ENSP00000331902.6:p.Ala1611=
ENST00000361603.6:c.4815A=	ENSP00000354505.2:p.Ala1605=
ENST00000504541.1:c.219+357A=	ENSP00000424845.1:n.219+357A=
ENST00000515658.1:c.325-1019A=
NM_000495.4:c.4815A=	NP_000486.1:p.Ala1605=
NM_033380.2:c.4833A=	NP_203699.1:p.Ala1611=
XM_005262070.2:c.4824A=	XP_005262127.1:p.Ala1608=
XM_006724616.2:c.4833A=	XP_006724679.1:p.Ala1611=
XM_011530849.1:c.4509A=	XP_011529151.1:p.Ala1503=
XM_011530851.1:c.2406A=	XP_011529153.1:p.Ala802=
XM_011530849.2:c.4848A=	XP_011529151.2:p.Ala1616=
XM_017029259.2:c.4839A=	XP_016884748.1:p.Ala1613=
XM_017029260.1:c.4830A=	XP_016884749.1:p.Ala1610=
XM_017029263.2:c.3168A=	XP_016884752.1:p.Ala1056=
NM_000495.5:c.4815A=	NP_000486.1:p.Ala1605=
NM_033380.3:c.4833A= MANE Select	NP_203699.1:p.Ala1611=