Canonical Allele Identifier: CA350865028

Gene: COL4A3 MFF-DT

Linked Data

• MyVariant Identifiers: chr2:g.228173679T>G (hg19) ; chr2:g.227308963T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227308963T>G , CM000664.2:g.227308963T>G	GRCh38
NC_000002.11:g.228173679T>G , CM000664.1:g.228173679T>G	GRCh37
NC_000002.10:g.227881923T>G	NCBI36
NG_011591.1:g.149399T>G , LRG_230:g.149399T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.1785T>G (COL4A3)
ENST00000683077.1:n.9T>G (COL4A3)
ENST00000684413.1:n.1967T>G (COL4A3)
ENST00000396578.8:c.4527T>G (COL4A3) MANE Select	ENSP00000379823.3:p.Asp1509Glu
ENST00000469504.2:c.434-241T>G (COL4A3)	ENSP00000493493.1:n.434-241T>G
ENST00000643388.1:c.213T>G (COL4A3)	ENSP00000495177.1:p.Asp71Glu
ENST00000396578.7:c.4527T>G (COL4A3)	ENSP00000379823.3:p.Asp1509Glu
ENST00000469504.1:n.149-241T>G (COL4A3)
NM_000091.4:c.4527T>G , LRG_230t1:c.4527T>G (COL4A3)	NP_000082.2:p.Asp1509Glu
NR_102371.1:n.48-3308A>C (MFF-DT)
XM_005246276.2:c.4527T>G (COL4A3)	XP_005246333.1:p.Asp1509Glu
XM_005246277.2:c.4422T>G (COL4A3)	XP_005246334.1:p.Asp1474Glu
XM_011510555.1:c.4527T>G (COL4A3)	XP_011508857.1:p.Asp1509Glu
XM_011510556.1:c.3288T>G (COL4A3)	XP_011508858.1:p.Asp1096Glu
XR_241280.2:n.4601-241T>G (COL4A3)
XM_005246277.3:c.4422T>G (COL4A3)	XP_005246334.1:p.Asp1474Glu
XM_011510556.2:c.3288T>G (COL4A3)	XP_011508858.1:p.Asp1096Glu
XR_241280.3:n.4601-241T>G (COL4A3)
NM_000091.5:c.4527T>G (COL4A3) MANE Select	NP_000082.2:p.Asp1509Glu