Canonical Allele Identifier: CA431663852

Gene: COL4A3 MFF-DT

Linked Data

• ClinVar Variation Id: 1631997
• ClinVar RCV Id: RCV002128210
• dbSNP Id: rs2073631640
• MyVariant Identifiers: chr2:g.228173736G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227309020G>T , CM000664.2:g.227309020G>T	GRCh38
NC_000002.11:g.228173736G>T , CM000664.1:g.228173736G>T	GRCh37
NC_000002.10:g.227881980G>T	NCBI36
NG_011591.1:g.149456G>T , LRG_230:g.149456G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.1842G>T (COL4A3)
ENST00000683077.1:n.66G>T (COL4A3)
ENST00000684413.1:n.2024G>T (COL4A3)
ENST00000396578.8:c.4584G>T (COL4A3) MANE Select	ENSP00000379823.3:p.Leu1528=
ENST00000469504.2:c.434-184G>T (COL4A3)	ENSP00000493493.1:n.434-184G>T
ENST00000643388.1:c.270G>T (COL4A3)	ENSP00000495177.1:p.Leu90=
ENST00000396578.7:c.4584G>T (COL4A3)	ENSP00000379823.3:p.Leu1528=
ENST00000469504.1:n.149-184G>T (COL4A3)
NM_000091.4:c.4584G>T , LRG_230t1:c.4584G>T (COL4A3)	NP_000082.2:p.Leu1528=
NR_102371.1:n.48-3365C>A (MFF-DT)
XM_005246276.2:c.4584G>T (COL4A3)	XP_005246333.1:p.Leu1528=
XM_005246277.2:c.4479G>T (COL4A3)	XP_005246334.1:p.Leu1493=
XM_011510555.1:c.4584G>T (COL4A3)	XP_011508857.1:p.Leu1528=
XM_011510556.1:c.3345G>T (COL4A3)	XP_011508858.1:p.Leu1115=
XR_241280.2:n.4601-184G>T (COL4A3)
XM_005246277.3:c.4479G>T (COL4A3)	XP_005246334.1:p.Leu1493=
XM_011510556.2:c.3345G>T (COL4A3)	XP_011508858.1:p.Leu1115=
XR_241280.3:n.4601-184G>T (COL4A3)
NM_000091.5:c.4584G>T (COL4A3) MANE Select	NP_000082.2:p.Leu1528=