Canonical Allele Identifier: CA1332835394

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227246733A= , CM000664.2:g.227246733A=	GRCh38
NC_000002.11:g.228111449A= , CM000664.1:g.228111449A=	GRCh37
NC_000002.10:g.227819693A=	NCBI36
NG_011591.1:g.87169A= , LRG_230:g.87169A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396578.8:c.436A= (COL4A3) MANE Select	ENSP00000379823.3:p.Ile146=
ENST00000396578.7:c.436A= (COL4A3)	ENSP00000379823.3:p.Ile146=
NM_000091.4:c.436A= , LRG_230t1:c.436A= (COL4A3)	NP_000082.2:p.Ile146=
NR_102371.1:n.1593-8559T= (MFF-DT)
XM_005246276.2:c.436A= (COL4A3)	XP_005246333.1:p.Ile146=
XM_005246277.2:c.436A= (COL4A3)	XP_005246334.1:p.Ile146=
XM_005246280.2:c.436A= (COL4A3)	XP_005246337.1:p.Ile146=
XM_006712245.2:c.436A= (COL4A3)	XP_006712308.1:p.Ile146=
XM_011510555.1:c.436A= (COL4A3)	XP_011508857.1:p.Ile146=
XR_241280.2:n.574A= (COL4A3)
XM_005246277.3:c.436A= (COL4A3)	XP_005246334.1:p.Ile146=
XM_005246280.3:c.436A= (COL4A3)	XP_005246337.1:p.Ile146=
XM_006712245.3:c.436A= (COL4A3)	XP_006712308.1:p.Ile146=
XM_017003295.1:c.436A= (COL4A3)	XP_016858784.1:p.Ile146=
XR_001738601.1:n.574A= (COL4A3)
XR_241280.3:n.574A= (COL4A3)
NM_000091.5:c.436A= (COL4A3) MANE Select	NP_000082.2:p.Ile146=