Canonical Allele Identifier: CA2450721581

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694841G= , CM000685.2:g.108694841G=	GRCh38
NC_000023.10:g.107938071G= , CM000685.1:g.107938071G=	GRCh37
NC_000023.9:g.107824727G=	NCBI36
NG_011977.1:g.259918G=
NG_011977.2:g.259918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4741G= MANE Select	ENSP00000331902.7:p.Ala1581=
ENST00000361603.7:c.4723G=	ENSP00000354505.2:p.Ala1575=
ENST00000510690.2:n.1235G=
ENST00000644079.1:n.1227G=
ENST00000328300.10:c.4741G=	ENSP00000331902.6:p.Ala1581=
ENST00000361603.6:c.4723G=	ENSP00000354505.2:p.Ala1575=
ENST00000504541.1:c.139G=	ENSP00000424845.1:p.Ala47=
ENST00000515658.1:c.325-1456G=
NM_000495.4:c.4723G=	NP_000486.1:p.Ala1575=
NM_033380.2:c.4741G=	NP_203699.1:p.Ala1581=
XM_005262070.2:c.4732G=	XP_005262127.1:p.Ala1578=
XM_006724616.2:c.4741G=	XP_006724679.1:p.Ala1581=
XM_011530849.1:c.4417G=	XP_011529151.1:p.Ala1473=
XM_011530851.1:c.2314G=	XP_011529153.1:p.Ala772=
XM_011530849.2:c.4756G=	XP_011529151.2:p.Ala1586=
XM_017029259.2:c.4747G=	XP_016884748.1:p.Ala1583=
XM_017029260.1:c.4738G=	XP_016884749.1:p.Ala1580=
XM_017029263.2:c.3076G=	XP_016884752.1:p.Ala1026=
NM_000495.5:c.4723G=	NP_000486.1:p.Ala1575=
NM_033380.3:c.4741G= MANE Select	NP_203699.1:p.Ala1581=