Canonical Allele Identifier: CA2754515299

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227312138T>A , CM000664.2:g.227312138T>A	GRCh38
NC_000002.11:g.228176854T>A , CM000664.1:g.228176854T>A	GRCh37
NC_000002.10:g.227885098T>A	NCBI36
NG_011591.1:g.152574T>A , LRG_230:g.152574T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.2539T>A (COL4A3)
ENST00000682257.1:n.503T>A (COL4A3)
ENST00000682970.1:n.579T>A (COL4A3)
ENST00000683077.1:n.2220T>A (COL4A3)
ENST00000684413.1:n.2848T>A (COL4A3)
ENST00000684724.1:n.702T>A (COL4A3)
ENST00000396578.8:c.*268T>A (COL4A3) MANE Select	ENSP00000379823.3:n.*268T>A
ENST00000396578.7:c.*268T>A (COL4A3)	ENSP00000379823.3:n.*268T>A
NM_000091.4:c.*268T>A , LRG_230t1:c.*268T>A (COL4A3)	NP_000082.2:n.*268T>A
NR_102371.1:n.48-6483A>T (MFF-DT)
XM_005246276.2:c.*194T>A (COL4A3)	XP_005246333.1:n.*194T>A
XM_005246277.2:c.*268T>A (COL4A3)	XP_005246334.1:n.*268T>A
XM_011510556.1:c.*268T>A (COL4A3)	XP_011508858.1:n.*268T>A
XR_241280.2:n.5241T>A (COL4A3)
XM_005246277.3:c.*268T>A (COL4A3)	XP_005246334.1:n.*268T>A
XM_011510556.2:c.*268T>A (COL4A3)	XP_011508858.1:n.*268T>A
XR_241280.3:n.5241T>A (COL4A3)
NM_000091.5:c.*268T>A (COL4A3) MANE Select	NP_000082.2:n.*268T>A