Canonical Allele Identifier: CA2450721785

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695439G= , CM000685.2:g.108695439G=	GRCh38
NC_000023.10:g.107938669G= , CM000685.1:g.107938669G=	GRCh37
NC_000023.9:g.107825325G=	NCBI36
NG_011977.1:g.260516G=
NG_011977.2:g.260516G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4994G= MANE Select	ENSP00000331902.7:p.Ser1665=
ENST00000361603.7:c.4976G=	ENSP00000354505.2:p.Ser1659=
ENST00000510690.2:n.1488G=
ENST00000644079.1:n.1825G=
ENST00000328300.10:c.4994G=	ENSP00000331902.6:p.Ser1665=
ENST00000361603.6:c.4976G=	ENSP00000354505.2:p.Ser1659=
ENST00000504541.1:c.219+518G=	ENSP00000424845.1:n.219+518G=
ENST00000515658.1:c.325-858G=
NM_000495.4:c.4976G=	NP_000486.1:p.Ser1659=
NM_033380.2:c.4994G=	NP_203699.1:p.Ser1665=
XM_005262070.2:c.4985G=	XP_005262127.1:p.Ser1662=
XM_006724616.2:c.4994G=	XP_006724679.1:p.Ser1665=
XM_011530849.1:c.4670G=	XP_011529151.1:p.Ser1557=
XM_011530851.1:c.2567G=	XP_011529153.1:p.Ser856=
XM_011530849.2:c.5009G=	XP_011529151.2:p.Ser1670=
XM_017029259.2:c.5000G=	XP_016884748.1:p.Ser1667=
XM_017029260.1:c.4991G=	XP_016884749.1:p.Ser1664=
XM_017029263.2:c.3329G=	XP_016884752.1:p.Ser1110=
NM_000495.5:c.4976G=	NP_000486.1:p.Ser1659=
NM_033380.3:c.4994G= MANE Select	NP_203699.1:p.Ser1665=