Canonical Allele Identifier: CA2450721729

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695290C= , CM000685.2:g.108695290C=	GRCh38
NC_000023.10:g.107938520C= , CM000685.1:g.107938520C=	GRCh37
NC_000023.9:g.107825176C=	NCBI36
NG_011977.1:g.260367C=
NG_011977.2:g.260367C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4845C= MANE Select	ENSP00000331902.7:p.Gly1615=
ENST00000361603.7:c.4827C=	ENSP00000354505.2:p.Gly1609=
ENST00000510690.2:n.1339C=
ENST00000644079.1:n.1676C=
ENST00000328300.10:c.4845C=	ENSP00000331902.6:p.Gly1615=
ENST00000361603.6:c.4827C=	ENSP00000354505.2:p.Gly1609=
ENST00000504541.1:c.219+369C=	ENSP00000424845.1:n.219+369C=
ENST00000515658.1:c.325-1007C=
NM_000495.4:c.4827C=	NP_000486.1:p.Gly1609=
NM_033380.2:c.4845C=	NP_203699.1:p.Gly1615=
XM_005262070.2:c.4836C=	XP_005262127.1:p.Gly1612=
XM_006724616.2:c.4845C=	XP_006724679.1:p.Gly1615=
XM_011530849.1:c.4521C=	XP_011529151.1:p.Gly1507=
XM_011530851.1:c.2418C=	XP_011529153.1:p.Gly806=
XM_011530849.2:c.4860C=	XP_011529151.2:p.Gly1620=
XM_017029259.2:c.4851C=	XP_016884748.1:p.Gly1617=
XM_017029260.1:c.4842C=	XP_016884749.1:p.Gly1614=
XM_017029263.2:c.3180C=	XP_016884752.1:p.Gly1060=
NM_000495.5:c.4827C=	NP_000486.1:p.Gly1609=
NM_033380.3:c.4845C= MANE Select	NP_203699.1:p.Gly1615=