Canonical Allele Identifier: CA2450721740

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695314T= , CM000685.2:g.108695314T=	GRCh38
NC_000023.10:g.107938544T= , CM000685.1:g.107938544T=	GRCh37
NC_000023.9:g.107825200T=	NCBI36
NG_011977.1:g.260391T=
NG_011977.2:g.260391T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4869T= MANE Select	ENSP00000331902.7:p.Pro1623=
ENST00000361603.7:c.4851T=	ENSP00000354505.2:p.Pro1617=
ENST00000510690.2:n.1363T=
ENST00000644079.1:n.1700T=
ENST00000328300.10:c.4869T=	ENSP00000331902.6:p.Pro1623=
ENST00000361603.6:c.4851T=	ENSP00000354505.2:p.Pro1617=
ENST00000504541.1:c.219+393T=	ENSP00000424845.1:n.219+393T=
ENST00000515658.1:c.325-983T=
NM_000495.4:c.4851T=	NP_000486.1:p.Pro1617=
NM_033380.2:c.4869T=	NP_203699.1:p.Pro1623=
XM_005262070.2:c.4860T=	XP_005262127.1:p.Pro1620=
XM_006724616.2:c.4869T=	XP_006724679.1:p.Pro1623=
XM_011530849.1:c.4545T=	XP_011529151.1:p.Pro1515=
XM_011530851.1:c.2442T=	XP_011529153.1:p.Pro814=
XM_011530849.2:c.4884T=	XP_011529151.2:p.Pro1628=
XM_017029259.2:c.4875T=	XP_016884748.1:p.Pro1625=
XM_017029260.1:c.4866T=	XP_016884749.1:p.Pro1622=
XM_017029263.2:c.3204T=	XP_016884752.1:p.Pro1068=
NM_000495.5:c.4851T=	NP_000486.1:p.Pro1617=
NM_033380.3:c.4869T= MANE Select	NP_203699.1:p.Pro1623=