Canonical Allele Identifier: CA350865205

Gene: COL4A3 MFF-DT

Linked Data

• MyVariant Identifiers: chr2:g.228173729C>G (hg19) ; chr2:g.227309013C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227309013C>G , CM000664.2:g.227309013C>G	GRCh38
NC_000002.11:g.228173729C>G , CM000664.1:g.228173729C>G	GRCh37
NC_000002.10:g.227881973C>G	NCBI36
NG_011591.1:g.149449C>G , LRG_230:g.149449C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.1835C>G (COL4A3)
ENST00000683077.1:n.59C>G (COL4A3)
ENST00000684413.1:n.2017C>G (COL4A3)
ENST00000396578.8:c.4577C>G (COL4A3) MANE Select	ENSP00000379823.3:p.Pro1526Arg
ENST00000469504.2:c.434-191C>G (COL4A3)	ENSP00000493493.1:n.434-191C>G
ENST00000643388.1:c.263C>G (COL4A3)	ENSP00000495177.1:p.Pro88Arg
ENST00000396578.7:c.4577C>G (COL4A3)	ENSP00000379823.3:p.Pro1526Arg
ENST00000469504.1:n.149-191C>G (COL4A3)
NM_000091.4:c.4577C>G , LRG_230t1:c.4577C>G (COL4A3)	NP_000082.2:p.Pro1526Arg
NR_102371.1:n.48-3358G>C (MFF-DT)
XM_005246276.2:c.4577C>G (COL4A3)	XP_005246333.1:p.Pro1526Arg
XM_005246277.2:c.4472C>G (COL4A3)	XP_005246334.1:p.Pro1491Arg
XM_011510555.1:c.4577C>G (COL4A3)	XP_011508857.1:p.Pro1526Arg
XM_011510556.1:c.3338C>G (COL4A3)	XP_011508858.1:p.Pro1113Arg
XR_241280.2:n.4601-191C>G (COL4A3)
XM_005246277.3:c.4472C>G (COL4A3)	XP_005246334.1:p.Pro1491Arg
XM_011510556.2:c.3338C>G (COL4A3)	XP_011508858.1:p.Pro1113Arg
XR_241280.3:n.4601-191C>G (COL4A3)
NM_000091.5:c.4577C>G (COL4A3) MANE Select	NP_000082.2:p.Pro1526Arg