Canonical Allele Identifier: CA2577265714

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227312011del , CM000664.2:g.227312011del	GRCh38
NC_000002.11:g.228176727del , CM000664.1:g.228176727del	GRCh37
NC_000002.10:g.227884971del	NCBI36
NG_011591.1:g.152447del , LRG_230:g.152447del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.2412del (COL4A3)
ENST00000682257.1:n.376del (COL4A3)
ENST00000682970.1:n.452del (COL4A3)
ENST00000683077.1:n.2093del (COL4A3)
ENST00000684413.1:n.2721del (COL4A3)
ENST00000684724.1:n.575del (COL4A3)
ENST00000396578.8:c.*141del (COL4A3) MANE Select	ENSP00000379823.3:n.*141del
ENST00000396578.7:c.*141del (COL4A3)	ENSP00000379823.3:n.*141del
NM_000091.4:c.*141del , LRG_230t1:c.*141del (COL4A3)	NP_000082.2:n.*141del
NR_102371.1:n.48-6353del (MFF-DT)
XM_005246276.2:c.*67del (COL4A3)	XP_005246333.1:n.*67del
XM_005246277.2:c.*141del (COL4A3)	XP_005246334.1:n.*141del
XM_011510556.1:c.*141del (COL4A3)	XP_011508858.1:n.*141del
XR_241280.2:n.5114del (COL4A3)
XM_005246277.3:c.*141del (COL4A3)	XP_005246334.1:n.*141del
XM_011510556.2:c.*141del (COL4A3)	XP_011508858.1:n.*141del
XR_241280.3:n.5114del (COL4A3)
NM_000091.5:c.*141del (COL4A3) MANE Select	NP_000082.2:n.*141del