Canonical Allele Identifier: CA431663870

Gene: COL4A3 MFF-DT

Linked Data

• ClinVar Variation Id: 2820278
• ClinVar RCV Id: RCV003709110
• MyVariant Identifiers: chr2:g.228173766C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227309050C>G , CM000664.2:g.227309050C>G	GRCh38
NC_000002.11:g.228173766C>G , CM000664.1:g.228173766C>G	GRCh37
NC_000002.10:g.227882010C>G	NCBI36
NG_011591.1:g.149486C>G , LRG_230:g.149486C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.1872C>G (COL4A3)
ENST00000683077.1:n.96C>G (COL4A3)
ENST00000684413.1:n.2054C>G (COL4A3)
ENST00000684724.1:n.16C>G (COL4A3)
ENST00000396578.8:c.4614C>G (COL4A3) MANE Select	ENSP00000379823.3:p.Gly1538=
ENST00000469504.2:c.434-154C>G (COL4A3)	ENSP00000493493.1:n.434-154C>G
ENST00000643388.1:c.300C>G (COL4A3)	ENSP00000495177.1:p.Gly100=
ENST00000396578.7:c.4614C>G (COL4A3)	ENSP00000379823.3:p.Gly1538=
ENST00000469504.1:n.149-154C>G (COL4A3)
NM_000091.4:c.4614C>G , LRG_230t1:c.4614C>G (COL4A3)	NP_000082.2:p.Gly1538=
NR_102371.1:n.48-3395G>C (MFF-DT)
XM_005246276.2:c.4614C>G (COL4A3)	XP_005246333.1:p.Gly1538=
XM_005246277.2:c.4509C>G (COL4A3)	XP_005246334.1:p.Gly1503=
XM_011510555.1:c.4614C>G (COL4A3)	XP_011508857.1:p.Gly1538=
XM_011510556.1:c.3375C>G (COL4A3)	XP_011508858.1:p.Gly1125=
XR_241280.2:n.4601-154C>G (COL4A3)
XM_005246277.3:c.4509C>G (COL4A3)	XP_005246334.1:p.Gly1503=
XM_011510556.2:c.3375C>G (COL4A3)	XP_011508858.1:p.Gly1125=
XR_241280.3:n.4601-154C>G (COL4A3)
NM_000091.5:c.4614C>G (COL4A3) MANE Select	NP_000082.2:p.Gly1538=