Canonical Allele Identifier: CA1332840319

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227257795_227257797delinsCTA , CM000664.2:g.227257795_227257797delinsCTA	GRCh38
NC_000002.11:g.228122511_228122513delinsCTA , CM000664.1:g.228122511_228122513delinsCTA	GRCh37
NC_000002.10:g.227830755_227830757delinsCTA	NCBI36
NG_011591.1:g.98231_98233delinsCTA , LRG_230:g.98231_98233delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396578.8:c.1029+151_1029+153delinsCTA (COL4A3) MANE Select	ENSP00000379823.3:n.1029+151_1029+153delinsCTA
ENST00000396578.7:c.1029+151_1029+153delinsCTA (COL4A3)	ENSP00000379823.3:n.1029+151_1029+153delinsCTA
NM_000091.4:c.1029+151_1029+153delinsCTA , LRG_230t1:c.1029+151_1029+153delinsCTA (COL4A3)	NP_000082.2:n.1029+151_1029+153delinsCTA
NR_102371.1:n.1592+1381_1592+1383delinsTAG (MFF-DT)
XM_005246276.2:c.1029+151_1029+153delinsCTA (COL4A3)	XP_005246333.1:n.1029+151_1029+153delinsCTA
XM_005246277.2:c.1029+151_1029+153delinsCTA (COL4A3)	XP_005246334.1:n.1029+151_1029+153delinsCTA
XM_005246280.2:c.1029+151_1029+153delinsCTA (COL4A3)	XP_005246337.1:n.1029+151_1029+153delinsCTA
XM_006712245.2:c.1029+151_1029+153delinsCTA (COL4A3)	XP_006712308.1:n.1029+151_1029+153delinsCTA
XM_011510555.1:c.1029+151_1029+153delinsCTA (COL4A3)	XP_011508857.1:n.1029+151_1029+153delinsCTA
XM_011510556.1:c.-207+151_-207+153delinsCTA (COL4A3)	XP_011508858.1:n.-207+151_-207+153delinsCTA
XR_241280.2:n.1167+151_1167+153delinsCTA (COL4A3)
XM_005246277.3:c.1029+151_1029+153delinsCTA (COL4A3)	XP_005246334.1:n.1029+151_1029+153delinsCTA
XM_005246280.3:c.1029+151_1029+153delinsCTA (COL4A3)	XP_005246337.1:n.1029+151_1029+153delinsCTA
XM_006712245.3:c.1029+151_1029+153delinsCTA (COL4A3)	XP_006712308.1:n.1029+151_1029+153delinsCTA
XM_011510556.2:c.-207+151_-207+153delinsCTA (COL4A3)	XP_011508858.1:n.-207+151_-207+153delinsCTA
XM_017003295.1:c.1029+151_1029+153delinsCTA (COL4A3)	XP_016858784.1:n.1029+151_1029+153delinsCTA
XR_001738601.1:n.1167+151_1167+153delinsCTA (COL4A3)
XR_241280.3:n.1167+151_1167+153delinsCTA (COL4A3)
NM_000091.5:c.1029+151_1029+153delinsCTA (COL4A3) MANE Select	NP_000082.2:n.1029+151_1029+153delinsCTA