Canonical Allele Identifier: CA2580065952

Gene: COL4A3 MFF-DT

Linked Data

• ClinVar Variation Id: 2016728
• ClinVar RCV Id: RCV002844043

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227253557T>C , CM000664.2:g.227253557T>C	GRCh38
NC_000002.11:g.228118273T>C , CM000664.1:g.228118273T>C	GRCh37
NC_000002.10:g.227826517T>C	NCBI36
NG_011591.1:g.93993T>C , LRG_230:g.93993T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396578.8:c.688-4T>C (COL4A3) MANE Select	ENSP00000379823.3:n.688-4T>C
ENST00000396578.7:c.688-4T>C (COL4A3)	ENSP00000379823.3:n.688-4T>C
NM_000091.4:c.688-4T>C , LRG_230t1:c.688-4T>C (COL4A3)	NP_000082.2:n.688-4T>C
NR_102371.1:n.1592+5621A>G (MFF-DT)
XM_005246276.2:c.688-4T>C (COL4A3)	XP_005246333.1:n.688-4T>C
XM_005246277.2:c.688-4T>C (COL4A3)	XP_005246334.1:n.688-4T>C
XM_005246280.2:c.688-4T>C (COL4A3)	XP_005246337.1:n.688-4T>C
XM_006712245.2:c.688-4T>C (COL4A3)	XP_006712308.1:n.688-4T>C
XM_011510555.1:c.688-4T>C (COL4A3)	XP_011508857.1:n.688-4T>C
XR_241280.2:n.826-4T>C (COL4A3)
XM_005246277.3:c.688-4T>C (COL4A3)	XP_005246334.1:n.688-4T>C
XM_005246280.3:c.688-4T>C (COL4A3)	XP_005246337.1:n.688-4T>C
XM_006712245.3:c.688-4T>C (COL4A3)	XP_006712308.1:n.688-4T>C
XM_017003295.1:c.688-4T>C (COL4A3)	XP_016858784.1:n.688-4T>C
XR_001738601.1:n.826-4T>C (COL4A3)
XR_241280.3:n.826-4T>C (COL4A3)
NM_000091.5:c.688-4T>C (COL4A3) MANE Select	NP_000082.2:n.688-4T>C