Canonical Allele Identifier: CA2450688805

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108598712C= , CM000685.2:g.108598712C=	GRCh38
NC_000023.10:g.107841942C= , CM000685.1:g.107841942C=	GRCh37
NC_000023.9:g.107728598C=	NCBI36
NG_011977.1:g.163789C=
NG_011977.2:g.163789C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.1790C= MANE Select	ENSP00000331902.7:p.Thr597=
ENST00000361603.7:c.1790C=	ENSP00000354505.2:p.Thr597=
ENST00000328300.10:c.1790C=	ENSP00000331902.6:p.Thr597=
ENST00000361603.6:c.1790C=	ENSP00000354505.2:p.Thr597=
ENST00000483338.1:n.1246C=
NM_000495.4:c.1790C=	NP_000486.1:p.Thr597=
NM_033380.2:c.1790C=	NP_203699.1:p.Thr597=
XM_005262070.2:c.1790C=	XP_005262127.1:p.Thr597=
XM_005262072.3:c.1790C=	XP_005262129.1:p.Thr597=
XM_006724616.2:c.1790C=	XP_006724679.1:p.Thr597=
XM_011530849.1:c.1466C=	XP_011529151.1:p.Thr489=
XM_011530850.1:c.1790C=	XP_011529152.1:p.Thr597=
XM_011530849.2:c.1805C=	XP_011529151.2:p.Thr602=
XM_017029259.2:c.1805C=	XP_016884748.1:p.Thr602=
XM_017029260.1:c.1805C=	XP_016884749.1:p.Thr602=
XM_017029261.1:c.1805C=	XP_016884750.1:p.Thr602=
XM_017029262.2:c.1805C=	XP_016884751.1:p.Thr602=
XM_017029263.2:c.125C=	XP_016884752.1:p.Thr42=
NM_000495.5:c.1790C=	NP_000486.1:p.Thr597=
NM_033380.3:c.1790C= MANE Select	NP_203699.1:p.Thr597=