Canonical Allele Identifier: CA1332862005

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227309175G= , CM000664.2:g.227309175G=	GRCh38
NC_000002.11:g.228173891G= , CM000664.1:g.228173891G=	GRCh37
NC_000002.10:g.227882135G=	NCBI36
NG_011591.1:g.149611G= , LRG_230:g.149611G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.1899-29G= (COL4A3)
ENST00000682257.1:n.7G= (COL4A3)
ENST00000683077.1:n.123-29G= (COL4A3)
ENST00000684413.1:n.2179G= (COL4A3)
ENST00000684724.1:n.43-10G= (COL4A3)
ENST00000396578.8:c.4641-29G= (COL4A3) MANE Select	ENSP00000379823.3:n.4641-29G=
ENST00000469504.2:c.434-29G= (COL4A3)	ENSP00000493493.1:n.434-29G=
ENST00000643388.1:c.327-29G= (COL4A3)	ENSP00000495177.1:n.327-29G=
ENST00000396578.7:c.4641-29G= (COL4A3)	ENSP00000379823.3:n.4641-29G=
ENST00000469504.1:n.149-29G= (COL4A3)
NM_000091.4:c.4641-29G= , LRG_230t1:c.4641-29G= (COL4A3)	NP_000082.2:n.4641-29G=
NR_102371.1:n.48-3520C= (MFF-DT)
XM_005246276.2:c.4641-29G= (COL4A3)	XP_005246333.1:n.4641-29G=
XM_005246277.2:c.4536-29G= (COL4A3)	XP_005246334.1:n.4536-29G=
XM_011510555.1:c.4641-29G= (COL4A3)	XP_011508857.1:n.4641-29G=
XM_011510556.1:c.3402-29G= (COL4A3)	XP_011508858.1:n.3402-29G=
XR_241280.2:n.4601-29G= (COL4A3)
XM_005246277.3:c.4536-29G= (COL4A3)	XP_005246334.1:n.4536-29G=
XM_011510556.2:c.3402-29G= (COL4A3)	XP_011508858.1:n.3402-29G=
XR_241280.3:n.4601-29G= (COL4A3)
NM_000091.5:c.4641-29G= (COL4A3) MANE Select	NP_000082.2:n.4641-29G=