Canonical Allele Identifier: CA1332861834

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227308756T= , CM000664.2:g.227308756T=	GRCh38
NC_000002.11:g.228173472T= , CM000664.1:g.228173472T=	GRCh37
NC_000002.10:g.227881716T=	NCBI36
NG_011591.1:g.149192T= , LRG_230:g.149192T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.1721-143T= (COL4A3)
ENST00000684413.1:n.1760T= (COL4A3)
ENST00000396578.8:c.4463-143T= (COL4A3) MANE Select	ENSP00000379823.3:n.4463-143T=
ENST00000469504.2:c.434-448T= (COL4A3)	ENSP00000493493.1:n.434-448T=
ENST00000643388.1:c.149-143T= (COL4A3)	ENSP00000495177.1:n.149-143T=
ENST00000396578.7:c.4463-143T= (COL4A3)	ENSP00000379823.3:n.4463-143T=
ENST00000469504.1:n.149-448T= (COL4A3)
NM_000091.4:c.4463-143T= , LRG_230t1:c.4463-143T= (COL4A3)	NP_000082.2:n.4463-143T=
NR_102371.1:n.48-3101A= (MFF-DT)
XM_005246276.2:c.4463-143T= (COL4A3)	XP_005246333.1:n.4463-143T=
XM_005246277.2:c.4358-143T= (COL4A3)	XP_005246334.1:n.4358-143T=
XM_011510555.1:c.4463-143T= (COL4A3)	XP_011508857.1:n.4463-143T=
XM_011510556.1:c.3224-143T= (COL4A3)	XP_011508858.1:n.3224-143T=
XR_241280.2:n.4601-448T= (COL4A3)
XM_005246277.3:c.4358-143T= (COL4A3)	XP_005246334.1:n.4358-143T=
XM_011510556.2:c.3224-143T= (COL4A3)	XP_011508858.1:n.3224-143T=
XR_241280.3:n.4601-448T= (COL4A3)
NM_000091.5:c.4463-143T= (COL4A3) MANE Select	NP_000082.2:n.4463-143T=