Canonical Allele Identifier: CA2450721586

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694854A= , CM000685.2:g.108694854A=	GRCh38
NC_000023.10:g.107938084A= , CM000685.1:g.107938084A=	GRCh37
NC_000023.9:g.107824740A=	NCBI36
NG_011977.1:g.259931A=
NG_011977.2:g.259931A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4754A= MANE Select	ENSP00000331902.7:p.Gln1585=
ENST00000361603.7:c.4736A=	ENSP00000354505.2:p.Gln1579=
ENST00000510690.2:n.1248A=
ENST00000644079.1:n.1240A=
ENST00000328300.10:c.4754A=	ENSP00000331902.6:p.Gln1585=
ENST00000361603.6:c.4736A=	ENSP00000354505.2:p.Gln1579=
ENST00000504541.1:c.152A=	ENSP00000424845.1:p.Gln51=
ENST00000515658.1:c.325-1443A=
NM_000495.4:c.4736A=	NP_000486.1:p.Gln1579=
NM_033380.2:c.4754A=	NP_203699.1:p.Gln1585=
XM_005262070.2:c.4745A=	XP_005262127.1:p.Gln1582=
XM_006724616.2:c.4754A=	XP_006724679.1:p.Gln1585=
XM_011530849.1:c.4430A=	XP_011529151.1:p.Gln1477=
XM_011530851.1:c.2327A=	XP_011529153.1:p.Gln776=
XM_011530849.2:c.4769A=	XP_011529151.2:p.Gln1590=
XM_017029259.2:c.4760A=	XP_016884748.1:p.Gln1587=
XM_017029260.1:c.4751A=	XP_016884749.1:p.Gln1584=
XM_017029263.2:c.3089A=	XP_016884752.1:p.Gln1030=
NM_000495.5:c.4736A=	NP_000486.1:p.Gln1579=
NM_033380.3:c.4754A= MANE Select	NP_203699.1:p.Gln1585=