Canonical Allele Identifier: CA350865055

Gene: COL4A3 MFF-DT

Linked Data

• MyVariant Identifiers: chr2:g.228173686A>G (hg19) ; chr2:g.227308970A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227308970A>G , CM000664.2:g.227308970A>G	GRCh38
NC_000002.11:g.228173686A>G , CM000664.1:g.228173686A>G	GRCh37
NC_000002.10:g.227881930A>G	NCBI36
NG_011591.1:g.149406A>G , LRG_230:g.149406A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.1792A>G (COL4A3)
ENST00000683077.1:n.16A>G (COL4A3)
ENST00000684413.1:n.1974A>G (COL4A3)
ENST00000396578.8:c.4534A>G (COL4A3) MANE Select	ENSP00000379823.3:p.Asn1512Asp
ENST00000469504.2:c.434-234A>G (COL4A3)	ENSP00000493493.1:n.434-234A>G
ENST00000643388.1:c.220A>G (COL4A3)	ENSP00000495177.1:p.Asn74Asp
ENST00000396578.7:c.4534A>G (COL4A3)	ENSP00000379823.3:p.Asn1512Asp
ENST00000469504.1:n.149-234A>G (COL4A3)
NM_000091.4:c.4534A>G , LRG_230t1:c.4534A>G (COL4A3)	NP_000082.2:p.Asn1512Asp
NR_102371.1:n.48-3315T>C (MFF-DT)
XM_005246276.2:c.4534A>G (COL4A3)	XP_005246333.1:p.Asn1512Asp
XM_005246277.2:c.4429A>G (COL4A3)	XP_005246334.1:p.Asn1477Asp
XM_011510555.1:c.4534A>G (COL4A3)	XP_011508857.1:p.Asn1512Asp
XM_011510556.1:c.3295A>G (COL4A3)	XP_011508858.1:p.Asn1099Asp
XR_241280.2:n.4601-234A>G (COL4A3)
XM_005246277.3:c.4429A>G (COL4A3)	XP_005246334.1:p.Asn1477Asp
XM_011510556.2:c.3295A>G (COL4A3)	XP_011508858.1:p.Asn1099Asp
XR_241280.3:n.4601-234A>G (COL4A3)
NM_000091.5:c.4534A>G (COL4A3) MANE Select	NP_000082.2:p.Asn1512Asp